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| Job Title |
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Clinical Project Manager – Late Phase (Respiratory) |
| Location |
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England, UK |
| Job Number |
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120249923 |
| Posted |
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07/02/2012 (18:19) |
| Agency/Employer |
|
i-Pharm Consulting |
Description
|
|
Clinical Project Manager - Late Phase (Respiratory)
A new and exciting opportunity has arisen for a Clinical Project Manager specifically in Late Phase studies. Working for one of the world's leading Pharmaceutical Services Company you will be responsible for managing and executing multiple regionally based clinical studies from initiation to closeout. You can be home or office based in the UK, Netherlands, Italy, France and Spain
LOCATION
UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey , Belgium, Germany, Italy, Netherlands, Spain
BENEFITS
Competitive Salary
Car Allowance & Bonus
Flexible working hours
Private Health Care
Life Insurance
Ongoing Training and Career Development Opportunities
ROLE/DESCRIPTION
As a Clinical Project Manager you will be expected to undertake full lifecycle responsibilities which will include:
* Lead the planning and implementation of cross functional project(s).
* Facilitate the definition of project scope, goals and deliverables.
* Define project tasks and resource requirements.
* Develop full scale cross functional project plans.
* Assemble and coordinate project staff.
* Manage project budget.
* Manage project resource allocation.
* Plan and schedule project timelines.
* Provide direction and support to cross functional project team.
* Overall project Quality Assurance.
* Constantly monitor and report on progress of the project to all stakeholders.
* Present reports defining project progress, problems and solutions.
* Implement and manage project changes and interventions to achieve project outputs.
* Produce project evaluations and assessment of results.
REQUIREMENTS
*A Life Science or Nursing Degree
*Experience in clinical research, including previous CRA and full service Project Management
*Experience in Project Management of late phase trials
*Candidates with Late Phase Pharma background can also be considered
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natalie Hall on +44 (0)20 3189 0463, or email (url removed). If this role is not suitable, Natalie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Clinical Project Manager / Project Manager / Late Phase Project Manager / CPM / PM / Clinical Project Leader / Clinical Research Associate / CRA / Clinical Research / Clinical Research Scientist / Project Manager / Clinical Project Director / Director of Clinical Operations / Clinical Study Manager / Pharma / CRO / Senior CPM / Lead CPM / UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / UK, Belgium
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Biostatistician - Berkshire |
| Location |
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Berkshire |
| Job Number |
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120249913 |
| Posted |
|
07/02/2012 (17:38) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Senior Biostatistician - Berkshire
This is an outstanding opportunity for a Biostatistician to join one of Europe's leading CROs. My client urgently requires a Biostatistician with PHASE I experience who is willing to work in Berkshire! This is an incredibly attractive role for any ambitious Biostatistician or any Senior Biostatistician looking for a new role at one of Europe's most ambitious and dynamic CROs. Apply now if you are a Biostatistician with massive ambition!
JOB TITLE
Senior Biostatistician - Berkshire
LOCATION
Berkshire
BENEFITS
Career Development
Ambitious company
High level of responsibility
ROLE/DESCRIPTION
My client is currently recruiting for a Senior Biostatistician at their Berkshire site. As a Senior Statistician, you would be responsible for providing a statistical analysis service and providing advice and assistance in the design of those studies. You will provide a contract statistics service to clients, including advice on design and appropriate statistical techniques.
Senior Statistician - Berkshire
We are currently recruiting for a Senior Statistician at our Berkshire site. As a Senior Statistician, you are responsible for providing a statistical analysis service and providing advice and assistance in the design of those studies. You will provide a contract statistics service to clients, including advice on design and appropriate statistical techniques. Other responsibilities and duties may include:
- Assume the role of Study Statistician for some studies, particularly non-standard / contract type studies.
- Development and review of Statistical Analysis Plans and Statistical Contributions, to include statistical methodology, statistical programming procedures, definition of derived variables, data handling rules and mock-ups.
- Statistical analysis of clinical trial data and related decision making.
- Responsible for statistical input to clinical study, pharmacokinetic and statistics reports.
- Maintain project administration files with regard to all documents produced by Biostatistics, including associated review, QC and project tracking information and internal and external communications.
- Review of protocols, providing a statistical advice service for internal and external clients.
- Scheduling of clinical statistical work to meet required deadlines. Ensuring that projects are completed in a timely and accurate manner.
- Perform QC of all efficacy and safety datasets and data displays.
- Review of Clinical Study Reports.
- Perform independent peer review of statistical deliverables.
- Provide statistical support to SAS Programmers.
REQUIREMENTS
You will possess an MSc in Statistics with ideally 3 years or more relevant statistical and programming experience. Relevant experience within a CRO or Pharma industry would be advantageous.
2-3 years experience in a CRO or pharma company in clinical research
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Consultant, Sam Stopp, on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Sam is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Senior Biostatistician / Biostatistician / Senior Statistician / Statistician / Berkshire / England / UK / CRO / Pharmaceutical Industry / Clinical Trials / CRO / Phase I / Study Statistician
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Clinical Quality Auditor, North West England |
| Location |
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North West England, North West |
| Job Number |
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120249907 |
| Posted |
|
07/02/2012 (17:31) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Clinical Quality Auditor, North West England
Clinical Quality Auditor required for a highly reputable Clinical Research Organisation based in North West England. As a key member of the Quality Department you will perform QA responsibilities, develop and implement global working practices and systems in compliance to GCP, enhance the reputation for the provision of quality of data and provide expert advice and service to customers.
JOB TITLE
Clinical Quality Auditor / QA Auditor / GCP Auditor
LOCATION
North West England / Manchester / Liverpool / Lancashire / Chester
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Perform Quality Assurance responsibilities including Internal Audits and Training to ensure consistency and compliance of operations
- Implement the Quality Management System
- To contribute to the development, improvement and implementation of global working practices and systems, in compliance with GCP and appropriate regulations
- Enhance the reputation for provision of quality of data
- Ensure patient care, well-being and confidentiality remain paramount
- Review patient complaints and resolutions, ensuring follow up
- Provide expert advice and service to customers
REQUIREMENTS
- BSc in scientific area (e.g. Biology) or related discipline
- Minimum of 2 years Clinical Quality auditing experience ideally including Europe
- Experience of MHRA, FDA or other regulatory authority inspections and sponsor audits
- High attention to detail and good organisational skills
- Ability to travel (including internationally) approximately 50% of the time
- Ability to work autonomously and as part of a team
- Good computer skills including experience of Microsoft software
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Clinical Quality Auditor / QA Auditor / GCP Auditor / North West England / Manchester / Liverpool / Lancashire / Chester
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Biostatistician - Yorkshire, England |
| Location |
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East Riding of Yorkshire, Humberside |
| Job Number |
|
120249906 |
| Posted |
|
07/02/2012 (17:30) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Senior Biostatistician - Yorkshire
This is an outstanding opportunity for a Biostatistician to join one of Europe's leading CROs. My client urgently requires a Biostatistician with PHASE I experience who is willing to work in Yorkshire! This is an incredibly attractive role for any ambitious Biostatistician or any Senior Biostatistician looking for a new role at one of Europe's most ambitious and dynamic CROs. Apply now if you are a Biostatistician with massive ambition!
JOB TITLE
Senior Biostatistician - Yorkshire
LOCATION
Yorkshire
BENEFITS
Career Development
Ambitious company
High level of responsibility
ROLE/DESCRIPTION
We are currently recruiting for a Senior Statistician at our Yorkshire site. As a Senior Statistician, you are responsible for providing a statistical analysis service and providing advice and assistance in the design of those studies. You will provide a contract statistics service to clients, including advice on design and appropriate statistical techniques.
Senior Statistician - Yorkshire
My client is currently recruiting for a Senior Statistician at their Yorkshire site. As a Senior Statistician, you would be responsible for providing a statistical analysis service and providing advice and assistance in the design of those studies. You would provide a contract statistics service to clients, including advice on design and appropriate statistical techniques.Other responsibilities and duties may include:
- Assume the role of Study Statistician for some studies, particularly non-standard / contract type studies.
- Development and review of Statistical Analysis Plans and Statistical Contributions, to include statistical methodology, statistical programming procedures, definition of derived variables, data handling rules and mock-ups.
- Statistical analysis of clinical trial data and related decision making.
- Responsible for statistical input to clinical study, pharmacokinetic and statistics reports.
- Maintain project administration files with regard to all documents produced by Biostatistics, including associated review, QC and project tracking information and internal and external communications.
- Review of protocols, providing a statistical advice service for internal and external clients.
- Scheduling of clinical statistical work to meet required deadlines. Ensuring that projects are completed in a timely and accurate manner.
- Perform QC of all efficacy and safety datasets and data displays.
- Review of Clinical Study Reports.
- Perform independent peer review of statistical deliverables.
- Provide statistical support to SAS Programmers.
REQUIREMENTS
You will possess an MSc in Statistics with ideally 3 years or more relevant statistical and programming experience. Relevant experience within a CRO or Pharma industry would be advantageous.
2-3 years experience in a CRO or pharma company in clinical research
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Sam Stopp on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Sam is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Senior Statistician / Statistician / CRO / Yokrshire / England / Pharmaceutical Industry / Biostatistics Department / Biostatistics / Statistics / Biostatistical / Statistical / SAS / Phase I / Clinical Trials
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Associate Director,Regulatory Affairs/Study Start Up,SE England |
| Location |
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England, UK |
| Job Number |
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120249896 |
| Posted |
|
07/02/2012 (17:16) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Associate Director, Regulatory Affairs / Study Start Up, South East England
Associate Director, Regulatory & Study Start Up, required to join a global Clinical Research Organisation. You will have line management responsibilities for a Regulatory team and be responsible for the development of regulatory business. Permanent opportunity based in South East England.
JOB TITLE
Associate Director, Regulatory & Study Start Up / Regulatory Affairs Manager / Regulatory Manager / Regulatory Affairs / Study Start Up
LOCATION
UK / South East England
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Line management of Regulatory team
- Coordination of projects and resources
- Contribute to discussions regarding the implementation of business strategy and set and implement site-specific objectives
- Financial responsibility and accountability for regulatory affairs sites
- Business development activities and risk analysis
- Write and review regulatory proposals
- Plan and deliver workshops or presentations on Regulatory Affairs topics
- Reviewer/Approver for Regulatory SOPs
REQUIREMENTS
- Degree in life science related discipline or professional equivalent
- At least 6 years regulatory experience including 3 years management experience
- Line management experience
- Ability to manage competing priorities
- Advanced negotiating and influencing skills
- Excellent communication and interpersonal skills
- Strong software and computer skills
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Associate Director, Regulatory & Study Start Up / Regulatory Affairs Manager / Regulatory Manager / Regulatory Affairs / Study Start Up / UK / South East England
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Regulatory Affairs Manager– Maidenhead, UK / home based – |
| Location |
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South East England, South East |
| Job Number |
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120249894 |
| Posted |
|
07/02/2012 (17:13) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Regulatory Affairs Manager- Maidenhead, UK / home based - 60K+
Regulatory Affairs Manager required for an exciting opportunity with a highly reputable Clinical Research Organisation. You will be responsible for leading the regulatory functions within a group setting. Office based in Maidenhead but part home based working happily considered for right candidates.
JOB TITLE
Regulatory Affairs Manager / Regulatory Affairs Director / RA Manager
LOCATION
Office based in Maidenhead but part home based working happily considered for right candidates
BENEFITS
60K+ plus benefits
ROLE/DESCRIPTION
- Lead regulatory functions within a group setting
- Management of global submissions (EU and CEE countries)
- Providing input to clinical strategies
- Reviewing clinical documentation for the planning of clinical development programs
- Compiling dossiers for marketing and product authorisation, including variations and notifications
- Preparation of IMPDs, compliance reviews of SmPCs
- Reviews of product labels and patient leaflets
- Supervising and coordinating regulatory advisors in local country offices
REQUIREMENTS
- Life science degree with at least three years of regulatory experience in EU countries
- CTA submission experience in at least 2 EU/CEE countries
- Fluent in written and spoken English and at least 1 other European language
- Some travel will be required
- Excellent communication, presentation skills
- Knowledge of MS office applications
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Regulatory Affairs Manager / Regulatory Affairs Director / RA Manager / UK / Maidenhead / home based
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Clinical Research Physician, North-West England |
| Location |
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North West England, North West |
| Job Number |
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120249889 |
| Posted |
|
07/02/2012 (17:10) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Senior Clinical Research Physician, North-West England
Senior Clinical Research Physician required for a highly reputable Clinical Research Organisation. This is an exciting opportunity for a GMC registered doctor with prior experience as a Principal Investigator in Phase I/Clinical Pharmacology studies. This role is based in the North-West of England.
JOB TITLE
Senior Clinical Research Physician / Senior Clinical Trial Physician / Investigator / Senior Research Physician / Clinical Research Physician / Clinical Trial Physician
LOCATION
UK / England / North West / NW / Manchester / Liverpool / Cheshire / Lancashire
BENEFITS
Generous Salary
Full Benefits Package
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- To provide medical support for the conduct of studies
- To act as Principal Investigator for clinical trials
- Supervision, training and mentoring of Clinical Research Physicians operating as sub-investigators
- To provide medical input into study protocols, interim reports, safety reports and final study reports, assisting project management with the leadership of studies and client liaison
- To assess the feasibility and clinical resource implications of all studies at an early stage of protocol development
- To develop and maintain a high level of skill in designing, conducting and interpreting clinical pharmacology studies
- To maintain level of skills necessary for the practice of clinical medicine
REQUIREMENTS
- MB ChB, MB BS or equivalent
- Full GMC registration in the UK
- Valid certificate in Advanced Life Support (ALS)
- Post-graduate qualification such as MRCO, Dip Pharm Med, MFPM, FFPM, DCOSA or equivalent desirable
- Prior relevant experience of direct patient care
- Prior experience as a Principal Investigator in Phase I/Clinical Pharmacology studies
- Experience in clinical trial methodology
- Thorough grounding in general medicine and a firm grasp of the basic principles of pharmacology and therapeutics
- Conversant with responsibilities under ICH-GCP and other relevant regulations and guidelines covering the conduct of clinical research including Clinical Trials Regulations and the Declaration of Helsinki
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Senior Clinical Research Physician / Senior Clinical Trial Physician / Investigator / Senior Research Physician / Clinical Research Physician / Clinical Trial Physician / UK / England / North West / NW / Manchester / Liverpool / Cheshire / Lancashire
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Quality Assurance Auditor, home based |
| Location |
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Berkshire |
| Job Number |
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120249885 |
| Posted |
|
07/02/2012 (17:06) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Senior Quality Assurance Auditor, home based
Senior Quality Assurance Auditor required for a highly reputable, muli-national Clinical Research Organisation. You will be responsible for performing international clinical site audits, conducting audits of data, reports and systems as well as generating audit plans and reports. This is a full time, home based position.
Senior Quality Assurance Auditor / Senior Clinical Quality Auditor / Senior QA Auditor / Senior GCP Auditor / Clinical Quality Auditor / QA Auditor / GCP Auditor
LOCATION
UK / England / Greater London / Reading / Berkshire (home based)
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Performing international clinical site audits
- Conducting audits of data and reports as well as systems audits
- Generation of audit plans and reports for clients and management
- Providing assistance within the organisation on ICH guidelines, FDA regulations, internal SOPs and other national guidelines/requirements
REQUIREMENTS
- Degree in a life science or nursing qualification or equivalent
- 3 years' experience of auditing in a GCP environment
- Extensive travel is required
- Excellent communication, interpersonal and IT skills are essential
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Senior Quality Assurance Auditor / Senior Clinical Quality Auditor / Senior QA Auditor / Senior GCP Auditor / Clinical Quality Auditor / QA Auditor / GCP Auditor / UK / England / Greater London / Reading / Berkshire (home based)
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Medical Writer, Global CRO |
| Location |
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Scotland |
| Job Number |
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120249877 |
| Posted |
|
07/02/2012 (16:28) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Senior Medical Writer, Global CRO
Senior Medical Writer required for a global Clinical Research Organisation. You will be responsible for a variety of clinical documents for a wide range of both international and local sponsors across all therapeutic areas. If you have experience within Medical Affairs, Regulatory Affairs or Medical Information and have excellent written communication skills please apply now! This is a Scotland based, permanent opportunity.
JOB TITLE
Senior Medical Writer / Medical Writer
LOCATION
UK / Scotland
BENEFITS
Competitive salary and benefits package
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Coordinate local and global writing teams for programs of studies
- Interact directly with international project team members and sponsor, proactively manage own deliverables and identify and respond appropriately with solutions to any potential issues and problems
- Identify project needs and create project timelines
- Mentor to junior staff
- Provide Senior Medical Writing review of deliverables
- May act as a Project Manager on a writing project
REQUIREMENTS
- Degree in science or health related discipline
- Prior experience in a Medical Writer role including extensive hands-on experience in preparing clinical study protocols and reports
- Excellent communication skills
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Senior Medical Writer / Medical Writer / UK / Scotland
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Medical Information Associate, Bulgaria |
| Location |
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Bulgaria, Non UK |
| Job Number |
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120249876 |
| Posted |
|
07/02/2012 (16:27) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Medical Information Associate, Bulgaria
Medical Information Associate required to join a global Clinical Research Organisation. You will provide technical and medical information on a wide range of pharmaceutical products to consumers and healthcare professionals (doctors and pharmacists). Bulgaria based role. Permanent opportunity.
JOB TITLE
Medical Information Associate / Medical Information Officer / Medical Information / Healthcare Compliance
LOCATION
Bulgaria / Sofia
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Reply to queries from health care professionals and patients over the phone
- Provide information according to protocols on new and existing products
- Accurately maintain the enquiry database and related documents
REQUIREMENTS
- A degree in Medicine, Pharmacy, Biology, Chemistry or nursing qualification
- Excellent knowledge of English and French is essential
- Good customer service and strong interpersonal skills
- Willingness to work to protocols and regulatory guidelines
- Familiarity with the use of MS Office packages
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Medical Information Associate / Medical Information Officer / Medical Information / Healthcare Compliance / Bulgaria / Sofia
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Medical Writer, Global CRO |
| Location |
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England, UK |
| Job Number |
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120249875 |
| Posted |
|
07/02/2012 (16:24) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Senior Medical Writer, Global CRO
Senior Medical Writer required for a global Clinical Research Organisation. You will be responsible for a variety of clinical documents for a wide range of both international and local sponsors across all therapeutic areas. If you have experience within Medical Affairs, Regulatory Affairs or Medical Information and have excellent written communication skills please apply now! This is a UK based, permanent opportunity.
JOB TITLE
Senior Medical Writer / Medical Writer
LOCATION
UK / England
BENEFITS
Competitive salary and benefits package
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Coordinate local and global writing teams for programs of studies
- Interact directly with international project team members and sponsor, proactively manage own deliverables and identify and respond appropriately with solutions to any potential issues and problems
- Identify project needs and create project timelines
- Mentor to junior staff
- Provide Senior Medical Writing review of deliverables
- May act as a Project Manager on a writing project
REQUIREMENTS
- Degree in science or health related discipline
- Prior experience in a Medical Writer role including extensive hands-on experience in preparing clinical study protocols and reports
- Excellent communication skills
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Senior Medical Writer / Medical Writer / UK / England
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Permanent |
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N/A |
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ASAP |
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Medical Information Associate, Bulgaria |
| Location |
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Bulgaria, Non UK |
| Job Number |
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120249873 |
| Posted |
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07/02/2012 (16:22) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Medical Information Associate, Bulgaria
Medical Information Associate required to join a global Clinical Research Organisation. You will provide technical and medical information on a wide range of pharmaceutical products to consumers and healthcare professionals (doctors and pharmacists). Bulgaria based role. Permanent opportunity.
JOB TITLE
Medical Information Associate / Medical Information Officer / Medical Information / Healthcare Compliance
LOCATION
Bulgaria / Sofia
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Reply to queries from health care professionals and patients over the phone
- Provide information according to protocols on new and existing products
- Accurately maintain the enquiry database and related documents
REQUIREMENTS
- A degree in Medicine, Pharmacy, Biology, Chemistry or nursing qualification
- Excellent knowledge of English and French is essential
- Good customer service and strong interpersonal skills
- Willingness to work to protocols and regulatory guidelines
- Familiarity with the use of MS Office packages
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Medical Information Associate / Medical Information Officer / Medical Information / Healthcare Compliance / Bulgaria / Sofia
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N/A |
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ASAP |
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Senior Clinical Data Manager/ Associate Director - Frankfurt |
| Location |
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Frankfurt am Main, Non UK |
| Job Number |
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120249819 |
| Posted |
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07/02/2012 (12:45) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Senior Clinical Data Manager - Frankfurt / Home-Based
JOB TITLE - Senior Clinical Data Manager
LOCATION - Frankfurt / Home-Based
My client requires a Senior Clinical Data Manager to join their German team! THIS POSITION CAN BE
HOME-BASED. This is a brilliant opportunity for a Data Manager looking for promotion, or a Senior Clinical Data Manager looking for a new challenge! This is a fantastic opportunity to join one of Europe's leading CROs! Apply now if you feel you are up to the challenge!
BENEFITS
Generous salary
Opportunity to work for one of Europe's leading CROs
Very high level of responsibility
ROLE/DESCRIPTION
The Sr. Manager provides guidance and general supervision to the Data Management team across projects. Monitors specified tasks to ensure quality and integrity of data. Executes the Data Management functions in accordance with Standard Operating Procedures (SOPs).
REQUIREMENTS
PREFERRED SKILLS:
*Bachelor's degree preferred
*Proven experience and in depth understanding of all aspects of Data Management
*Proven supervisory experience
*Computer literacy
*Accurate keyboard skills
*Good understanding of medical terminology
*Experience of the clinical research process and terminology
*Effective communication skills including coordination skills, good personal presentation, oral and written communication skills
*Experience working in a team environment under time and resource pressures
*Understanding the principles of ICH-GCP
KEY ATTRIBUTES:
*Good communication skills when working with sponsors and supporting colleagues
*Able to organize multiple ongoing tasks, and understand the differing priorities
*Proven experience in clinical research with a strong knowledge of SOPs and accepted practices
*Good understanding of the work performed by other Chiltern International functions and how they interact
*Previous experience in Data Management
*Confident dealing with external and internal sponsors
*Able to be proactive and use initiative
*Able to organize multiple ongoing tasks, and understand the differing priorities
*Proven ability for working independently with minimal supervision
*Proven experience of good interpersonal skills
*Experience of line management and staff supervision
*Possess good presentation skills
*Budgetary and financial awareness
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant, Sam Stopp, on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Sam is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
SAS Programmer / Statistical Programmer / Biostatistical Programmer / SAS Programming / Base / Macro / SAS / Tables / Listings / Graphs / TLG / SAS Programmer II / CRO / Pharmaceutical / Statistician / Biostatistical Programmer / Biostatistics/ Senior SAS Programmer / Principal SAS Programmer/ Germany / Home-Based / Clinical Data Manager / Senior Clinical Data Manager / Clinical Data Associate / Frankfurt
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N/A |
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ASAP |
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Biostatistician - Cambridgeshire |
| Location |
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Cambridge, Cambridgeshire |
| Job Number |
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120249815 |
| Posted |
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07/02/2012 (12:12) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Biostatistician / Statistician - Cambridgeshire
My client is looking for talented and ambitious biostatisticians to join their Biostatistics / Statistics Department in Cambridgeshire. This is an excellent opportunity for career progression, as you will be joining one of Europe's leading CROs, as well as a growing and dynamic Biostatistics / Statistics Department.
JOB TITLE - Biostatistician / Statistician
LOCATION - Cambridgeshire
ROLE/DESCRIPTION
The Biostatistics department are looking for a Statistician.
A head for figures can help save lives. Your programming skills could benefit millions of people across the globe.
Working on behalf of major pharmaceutical, biotechnology and medical device companies in support of clinical trials, you will liaise closely with our statisticians, programmers, data managers and multidisciplinary project teams to provide statistical expertise for reporting clinical trial data using suitable analyses, data summaries, listings and figures.
We are looking to recruit a statistician to join our Biostatistics and Programming team. Your role will be to support the lead statistician or lead programmer on projects, by providing statistical support for data summaries and analyses. To suggest developments to tools and techniques for improving process efficiencies and to represent the Biostatistics and Programming department within the company and with client companies and regulatory agencies, as required.
Other tasks will include ensuring projects are well documented consistent with company SOPs and working practices, time management of own and team's time spent on projects and interaction with the sponsor on programming aspects of the project.
REQUIREMENTS
To be considered for this role you will ideally have a MSc or BSc degree with a strong statistics content. You will also have good data analysis and SAS® programming skills and have familiarity with ICH Statistical and reporting guidelines and GCP. You should have good organizational skills of own work load with the ability to adapt and adjust to changing priorities.
Excellent written and verbal communication skills are a must.
Sound like you? We are seeking highly motivated and skilled candidates who will want to
share in our continued growth in the international market place.
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Sam Stopp on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Sam is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Biostatistician / Statistician / SAS / Hampshire / Biostatistics Degree / SAS Programmer / Biostatistical / Statistical / Biostatistics Department / Statistical Department / CRO / Pharmaceutical Statistics / Statistical Specialist / ICH Statistical / Biostatistics Team / Programming Team / Biotechnology / Medical Device / Lead Statistician / Project Manager / Support / Statistical Support / Tables / Listings / Graphs / Base / Macro / Cambridgeshire
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Biostatistician - Cambridgeshire |
| Location |
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Cambridge, Cambridgeshire |
| Job Number |
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120249814 |
| Posted |
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07/02/2012 (12:11) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
|
|
Biostatistician / Statistician - Cambridgeshire
My client is looking for talented and ambitious biostatisticians to join their Biostatistics / Statistics Department in Cambridgeshire. This is an excellent opportunity for career progression, as you will be joining one of Europe's leading CROs, as well as a growing and dynamic Biostatistics / Statistics Department.
JOB TITLE - Biostatistician / Statistician
LOCATION - Cambridgeshire
ROLE/DESCRIPTION
The Biostatistics department are looking for a Statistician.
A head for figures can help save lives. Your programming skills could benefit millions of people across the globe.
Working on behalf of major pharmaceutical, biotechnology and medical device companies in support of clinical trials, you will liaise closely with our statisticians, programmers, data managers and multidisciplinary project teams to provide statistical expertise for reporting clinical trial data using suitable analyses, data summaries, listings and figures.
We are looking to recruit a statistician to join our Biostatistics and Programming team. Your role will be to support the lead statistician or lead programmer on projects, by providing statistical support for data summaries and analyses. To suggest developments to tools and techniques for improving process efficiencies and to represent the Biostatistics and Programming department within the company and with client companies and regulatory agencies, as required.
Other tasks will include ensuring projects are well documented consistent with company SOPs and working practices, time management of own and team's time spent on projects and interaction with the sponsor on programming aspects of the project.
REQUIREMENTS
To be considered for this role you will ideally have a MSc or BSc degree with a strong statistics content. You will also have good data analysis and SAS® programming skills and have familiarity with ICH Statistical and reporting guidelines and GCP. You should have good organizational skills of own work load with the ability to adapt and adjust to changing priorities.
Excellent written and verbal communication skills are a must.
Sound like you? We are seeking highly motivated and skilled candidates who will want to
share in our continued growth in the international market place.
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Sam Stopp on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Sam is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Biostatistician / Statistician / SAS / Hampshire / Biostatistics Degree / SAS Programmer / Biostatistical / Statistical / Biostatistics Department / Statistical Department / CRO / Pharmaceutical Statistics / Statistical Specialist / ICH Statistical / Biostatistics Team / Programming Team / Biotechnology / Medical Device / Lead Statistician / Project Manager / Support / Statistical Support / Tables / Listings / Graphs / Base / Macro / Cambridgeshire
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Permanent |
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N/A |
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ASAP |
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Medical Affairs Operations Manager, Switzerland |
| Location |
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Basel, Non UK |
| Job Number |
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120249784 |
| Posted |
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07/02/2012 (10:50) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Medical Affairs Operations Manager, Switzerland
Medical Affairs Operations Manager responsible for planning and tracking of key Global Medical Affairs Team activities of one or more brands, including timelines, budgets, study/activities, progress updates, contracts, regular reporting. This is a 6 month contract role based in Basel.
JOB TITLE
Medical Affairs Operations Manager, Operations Manager
LOCATION
Switzerland / Basel
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Medical Affairs Team Project Management
- Finance and Resource Management including the preparation of regular budget reviews and coordination of yearly budget development
- Support generation of complete, high quality, Medical Affairs sub-plans that reflect the overall agreed brand strategy
- Track execution of Global Medical Affairs Team deliverables regarding budgets (external cost) and progress (timelines, issues, mitigation activities).
- Generate progress reports, highlight deviations
- Maintain all Medical Affairs Team documentation, objectives, ensure accuracy of key Global Medical Affairs Team data.
REQUIREMENTS
- Bachelors degree in life science and business management training or experience
- 4 years experience in a multidisciplinary environment or in line function (drug development)
- Excellent communication skills, written and verbal
- Fluent English
- Basic level knowledge of basic science and basic understanding of global drug development process
- Advanced planning and tracking skills with attention to detail, capable of managing multiple projects in early or late phase
- Excellent time management skills
- Strong interpersonal skills and quick action taker
- Analytical and logical thinker
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natasha Sandery on +44 (0)20 3189 0464, or email (url removed). If this role is not suitable, Natasha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Medical Affairs Operations Manager / Operations Manager / Switzerland / Basel
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Contract |
| Contract Length |
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6 months |
| Start Date |
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ASAP |
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Clinical Project Manager – (Psychiatry) Europe home based |
| Location |
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England, UK |
| Job Number |
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120249752 |
| Posted |
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06/02/2012 (18:22) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Clinical Project Manager - (Psychiatry) Europe home based
JOB SUMMARY
A Clinical Project Manager is required by a reputable and global Top 10 CRO to manage its Psychiatry Trials. The role will involve extensive management of regionally based clinical trials, and ensuring that all project requirements are completed to the sponsor's requirement. Flexible and home based arrangements for Project Manager's can be provided for, locations in UK and Europe.
JOB TITLE
Clinical Project Manager / Project Manager / Project Manager (Psychiatry) / Clinical Project Leader
LOCATION
UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / London UK / Netherlands / Spain / Belgium / France/ Netherlands
BENEFITS
Competitive Salary
Car Allowance & Bonus
Flexible working hours
Private Health Care
Life Insurance
Ongoing Training and Career Development Opportunities
ROLE/DESCRIPTION
As a Clinical Project Manager you will be expected to undertake full lifecycle responsibilities which will include:
* Manage and co-ordinate cross functional teams, manages study issues, maintain compliance standards in accordance with GCP and initiate study improvements for assigned projects.
*Develop Study management plans, Budget management, resource procurement and planning as well as project implementation.
* Collaborating with other functional groups to co-ordinate and manage study issues.
* Client interactions -liaising with sponsor development updates and meetings.
*Participate in proposal development teams and represent at marketing and new business meetings.
* Providing input to line managers on team performance and recommended team members further development, as well as acting as a mentor for Junior CPM's and CRA team.
*Lead problem solving, and resolution efforts including risk management. Identifying quality issues and implementing corrective measures.
REQUIREMENTS
* A Bachelor Degree in Life Science or related field
* Experience in clinical research, including previous CRA and Project Management Experience.
* Experience in Psychiatry therapy area and/or CRO sector experience is desirable.
* In depth knowledge in GCP - ICH guidelines
*Good teamwork, customer service and presentation skills
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natalie Hall on +44 (0)20 3189 0463, or email (url removed). If this role is not suitable, Natalie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Clinical Project Manager / Project Manager / CPM / PM / Clinical Project Leader / / Project Manager / Clinical Project Director / Director of Clinical Operations / Clinical Study Manager / Pharma / CRO / Senior CPM / Lead CPM UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / London / UK / Netherlands / Spain / Belgium / France/ Netherlands/ Psychiatry
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Permanent |
| Contract Length |
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N/A |
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ASAP |
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Director of Clinical Project Management, Late Phase (Phase IV) |
| Location |
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England, UK |
| Job Number |
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120249751 |
| Posted |
|
06/02/2012 (18:18) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Director of Clinical Project Management, Late Phase (Phase IV) RESPIRATORY /COPD
JOB SUMMARY
Experienced Director of Clinical Project Management professional with proven track record of managing Late Phase (Phase IV) Clinical Research projects required by Global CRO as part of strategy to grow their European Late Phase team. This position can be based (home OR office) from any of the major European locations including the UK, Germany, France, Belgium, the Netherlands, Italy, Spain and Poland.
Job Title
Director of Clinical Project Management Director of Clinical Research Clinical Research Director
Background (Company)
Major Global CRO with offices across Europe is growing its Late Phase Project Management group in response to increased demand for peri and post approval studies, specifically managing studies in Respiratory and COPD.
Key Responsibilities
You will direct the delivery of clinical projects/programs within the Late Phase Clinical Research group
You'll provide leadership to a late Phase Project Management group
BENEFITS
Competitive Salary
Car Allowance
Pension
Private Healthcare
Life Assurance
Flexible working arrangements
Welcoming and inclusive company culture
QUALIFICATIONS
Life Sciences Degree OR Nursing Qualification
Extensive (10+yrs) Clinical Project Management experience
Significant experience of Late Phase (Phase IV) Clinical Research projects
Experience in managing studies in Respiratory or COPD therapy area
Strong leadership skills
Experience managing budgets and timelines
Experience managing groups of Clinical Project Managers
Experience of International Clinical Trials
To Apply
If you would like to discuss this vacancy further, please call Principal Consultant Natalie Hall on +44 (0)20 3189 0463, or email (url removed). If this role is not suitable, Natalie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
About i-Pharm Consulting
i-Pharm Consulting is a specialist recruitment company focused on mid to high-level roles in Clinical Research & Medical Affairs. We recruit for both permanent and contract staff across the UK & Europe. Our clients include Pharmaceutical, Biotechnology, Contract Research and Medical Device companies.
Key Words
Director of Clinical Project Management, Director of Clinical Research, Clinical Project Director, Oncology, Clinical Project Manager, Clinical Research Director, Late Phase, Phase IV, Peri-Approval, Post-Approval, Respiratory, COPD
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Permanent |
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N/A |
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APAP |
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Associate Director of Clinical Project Management -Rheumatology |
| Location |
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England, UK |
| Job Number |
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120249749 |
| Posted |
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06/02/2012 (18:12) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Associate Director of Clinical Project Management - (Rheumatology) Europe based
JOB SUMMARY
Associate Director of Clinical Project Management is required by a reputable and global Top 5 CRO to manage its Rheumatology Trials within the Internal Medicine Clinical Project Management Department. You would be responsible for managing and co-ordinating the cross functional studies, ensuring that all study management and project deliverables are completed to the Sponsor's requirement.
JOB TITLE
Associate Director of Clinical Project Management (Rheumatology)
LOCATION
UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / London /Bulgaria / Italy / Poland / Belgium / Greece / France / Netherlands
BENEFITS
Competitive Salary
Car Allowance & Bonus
Flexible working hours
Private Health Care
Life Insurance
Ongoing Training and Career Development Opportunities
ROLE/DESCRIPTION
As a Clinical Project Manager you will be expected to undertake full lifecycle responsibilities which will include:
* Manage and co-ordinate cross functional teams, manages study issues, maintain compliance
* Collaborating with other functional groups to co-ordinate and manage study issues.
* Client interactions, primary point of contact -liaising with sponsor development updates and meetings.
*Proposal development teams and represent at marketing and new business meetings.
REQUIREMENTS
* A Bachelor Degree in Life Science or related field
* Experience in clinical research, including previous CRA and Project Management Experience.
* Experience in Internal Medicine including Rheumatology therapy area and/or CRO sector experience is desirable.
* In depth knowledge in GCP - ICH guidelines
*Good teamwork, customer service and presentation skills
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natalie Hall on +44 (0)20 3189 0463, or email (url removed). If this role is not suitable, Natalie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Associate Director of Clinical Project Management / CPM / PM / Clinical Project Leader / Clinical Research Associate / CRA / Clinical Research / Clinical Research Scientist / Project Manager / Clinical Project Director / Director of Clinical Operations / Clinical Study Manager / Pharma / CRO / Senior CPM / Lead CPM / UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / London / Rheumatology / London /Bulgaria / Italy / Poland / Belgium / Greece / France / Netherlands
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Permanent |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Clinical Project Manager - Early Phase |
| Location |
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Cardiff, Wales |
| Job Number |
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120249748 |
| Posted |
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06/02/2012 (18:03) |
| Agency/Employer |
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i-Pharm Consulting |
| Description
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Clinical Project Manager - Early Phase
A new and exciting opportunity has arisen for a Clinical Project Manager specifically in Early Phase studies. Working for a niche Pharmaceutical Services Company you will be responsible for managing and executing multiple regionally based clinical studies from initiation to closeout. Ideally you will be office based in Cardiff, Wales
LOCATION
Cardiff, Wales
BENEFITS
Competitive Salary
Car Allowance & Bonus
Flexible working hours
Private Health Care
Life Insurance
Ongoing Training and Career Development Opportunities
ROLE/DESCRIPTION
As an Early Phase Clinical Project Manager you will be expected to undertake full lifecycle responsibilities which will include:
* Lead the planning and implementation of cross functional project(s).
* Facilitate the definition of project scope, goals and deliverables.
* Define project tasks and resource requirements.
* Develop full scale cross functional project plans.
* Assemble and coordinate project staff.
* Manage project budget.
* Manage project resource allocation.
* Plan and schedule project timelines.
* Provide direction and support to cross functional project team.
* Overall project Quality Assurance.
* Constantly monitor and report on progress of the project to all stakeholders.
* Present reports defining project progress, problems and solutions.
* Implement and manage project changes and interventions to achieve project outputs.
* Produce project evaluations and assessment of results.
REQUIREMENTS
*A Life Science or Nursing Degree
*Experience in Project Management of early phase trials
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
(url removed)
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Natalie Hall on +44 (0)20 3189 0463, or email (url removed). If this role is not suitable, Natalie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Clinical Project Manager / Project Manager / Late Phase Project Manager / CPM / PM / Clinical Project Leader / Clinical Research Associate / CRA / Clinical Research / Clinical Research Scientist / Project Manager / Clinical Project Director / Director of Clinical Operations / Clinical Study Manager / Pharma / CRO / Early Phase / Phase 1/ Phase I/Wales / Cardiff
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Permanent |
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N/A |
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