 |
| Job Title |
|
Medical Director, Endocrinologist |
| Location |
|
England, UK |
| Job Number |
|
120250147 |
| Posted |
|
09/02/2012 (12:22) |
| Agency/Employer |
|
i-Pharm Consulting |
Description
|
|
Medical Director, Endocrinologist
Medical Director, Endocrinologist required for a leading Global Clinical Research Organisation. You will provide medical, clinical, and scientific advisory expertise and participate in all aspects of Medical and Scientific Services' involvement on assigned trials. Permanent role, Europe based.
JOB TITLE
Medical Director/ Endocrinologist / Principle Investigator / PI / P.I. / Senior Research Physician
LOCATION
Europe
BENEFITS
Generous Salary
Full Benefits Package
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Regional Medical Advisor on assigned projects
- Provide medical support to investigative sites and project staff for protocol-related issues
- Review and clarification of trial-related Adverse Events (AEs)
- Medical case review of Serious Adverse Events (SAEs)
- Provide medical support for the Analysis Of Similar Events (AOSE)
- Medical review of Adverse Event coding
- Medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs)
- Review of the Clinical Study Report (CSR) and patient narratives
- On call 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites
- Attend and present at Investigator Meetings
- Provide therapeutic area/indication training for the project clinical team
- Serve as Scientific Advisor and provide guidance to Project Managers on the medical and scientific aspects of assigned projects
- Strategic business development activities including presentations to prospective clients, professional meetings, and other business development activities for Medical & Scientific Services
REQUIREMENTS
- Medical degree along with a medical license from the country or region in which he/she resides
- Minimum of 5 years experience in clinical medicine, inclusive of post-graduate medical education
- Clinical development experience in the Pharmaceutical, CRO, or Biotech industry and knowledge of drug and device safety regulations preferred
- Specialty Board certification or equivalent combination of education, training and experience is desirable
- Excellent time management skills with an ability to establish priorities and meet deadlines in a demanding environment
- Skills in providing consultation and advice on multiple assignments as well as initiative and flexibility
- Strong interpersonal skills to be able to establish and maintain effective working relationships
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 31890464, or email (url removed). If this role is not suitable, Stephen is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Medical Director/ Endocrinologist / Principle Investigator / PI / P.I. / Senior Research Physician / Europe
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
 |
|
|
|
|
|
| Job Title |
|
SAS Programmer (Home Based) |
| Location |
|
England, UK |
| Job Number |
|
120250089 |
| Posted |
|
09/02/2012 (08:58) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
* Develop and review SAS programs and output for the management and reporting of clinical trial data
* Electronic Data Transfer
* SAS Set up
* Review draft and final production runs for projects to ensure quality and consistency
* Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
* Advise Senior Statistical Programming staff of changes in scope of projects to enable the timely development of change orders.
* Demonstrate good problem solving skills, a proactive approach and a willingness to take decisions, seeking advice from senior Statistical Programming staff to confirm decisions when necessary.
* With sufficient experience assume the role of a Lead Programmer for assigned projects.
* Ensure the filing of study documentation is maintained to the standard required according to processes and acceptable for audit.
* Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
* Involved in optimizing staff utilization and defining good practices
Profile :
Degree
3 years experience in Statistical Programming
Experience in Clinical Research and good understanting of the different roles involved in Clinical Trials
Autonomous
Excellent organisation skills
An understanding of the fundamental principles of programming, program development and review
Experience in the preparation of Programming Plans, study set-up and review of study specific documents
Location : Home Based
Duration : 3 to 6 months +
For a confidential conversation, feel free to get in touch with Fuanasa Maleo on +44 203 189 0461 or (url removed)
Keywords : SAS, R&D, Pharma, Biometrics, Bioinformatics
|
| Job Type |
|
Contract |
| Contract Length |
|
6 Months + |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
SAS Programmer |
| Location |
|
England, UK |
| Job Number |
|
120250088 |
| Posted |
|
09/02/2012 (08:51) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
SAS Programmer
* Develop and review SAS programs and output for the management and reporting of clinical trial data
* Electronic Data Transfer
* SAS Set up
* Review draft and final production runs for projects to ensure quality and consistency
* Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
* Advise Senior Statistical Programming staff of changes in scope of projects to enable the timely development of change orders.
* Demonstrate good problem solving skills, a proactive approach and a willingness to take decisions, seeking advice from senior Statistical Programming staff to confirm decisions when necessary.
* With sufficient experience assume the role of a Lead Programmer for assigned projects.
* Ensure the filing of study documentation is maintained to the standard required according to processes and acceptable for audit.
* Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
* Involved in optimizing staff utilization and defining good practices
Profile :
Degree
3 years experience in Statistical Programming
Experience in Clinical Research and good understanting of the different roles involved in Clinical Trials
Autonomous
Excellent organisation skills
An understanding of the fundamental principles of programming, program development and review
Experience in the preparation of Programming Plans, study set-up and review of study specific documents
Location : England
Duration : 3 to 6 months +
For a confidential conversation, feel free to get in touch with Fuanasa Maleo on +44 203 189 0461 or (url removed)
|
| Job Type |
|
Contract |
| Contract Length |
|
6 Months + |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Database Programmer - Yorkshire |
| Location |
|
South Yorkshire |
| Job Number |
|
120250080 |
| Posted |
|
08/02/2012 (18:39) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Clinical Database Programmer - Yorkshire
Clinical Database Programmer required! An excellent opportunity for Clinical Database Programmers at one of Europe's leading biometrics companies. This is an office-based role in Yorkshire. In this exciting role you will be providing technical expertise for the conduct of clinical trials across a broad range of therapy areas.
JOB TITLE:
Clinical Database Programmer / SAS Programmer / Programmer / Clinical Systems Programmer / Support Programmer
ROLE
*Provide technical expertise for the conduct of clinical trials to support various programming activities related to clinical systems within eClinical technologies.
*This role will involve both Database Programming and/or Clinical Systems & Support Programming depending on workload and experience
REQUIRED SKILLS
*Proficiency in at least one of the following programming languages : SAS, CDMS, EDC, SQL, VB, Java.
*Experience working with at least one system used in the clinical trial process (e.g. SAS, CDMS, EDC systems such as Inform, RAVE, Datalabs, CTMS etc.
*Clinical Trials/Pharmaceutical sector experience (including knowledge of ICH-GCP)
*Relevant degree
*Ability to learn new systems and function
LOCATION
Yorkshire/ England / UK
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, Samuel Stopp, on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Samuel is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
SAS / Clinical Database Programmer / SAS Programmer / Programmer / Clinical Systems Programmer / Support Programmer / England/ Yorkshire / SAS / CDMS / EDC / SQL / VB / Java / RAVE / Datalabs / CTMS
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Project Manager |
| Location |
|
England, UK |
| Job Number |
|
120250079 |
| Posted |
|
08/02/2012 (18:38) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Clinical Project Manager
JOB SUMMARY
Experienced Clinical Project Manager required by an already established and rapidly expanding CRO. This role can be home-based OR office-based in the UK. The UK offices are situated in Ascot, UK.
Job Title
Clinical Project Manager / Senior Clinical Project Manager
Background (Company)
With offices in 40 countries across 5 continents, you'll be joining an organisation with a genuinely global footprint.
Key Responsibilities
Managing European and Global Clinical Trials
Responsibility for timelines, budgets and regulatory compliance
Participate in bid defence and business development activities
Benefits
Competitive Salary
Car Allowance
Comprehensive Benefits Package
Qualifications
Life Sciences Degree
Extensive Clinical Project Management experience in a CRO environment
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
Clinical Project Manager / CPM / Senior Clinical PM/ Clinical Program Director, Clinical Project Director, Senior Clinical Project Manager, Clinical Project Manager, CPM, CPD, CRO
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Database Programmer - Berlin |
| Location |
|
Berlin, Non UK |
| Job Number |
|
120250078 |
| Posted |
|
08/02/2012 (18:34) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Clinical Database Programmer - Berlin
Clinical Database Programmer required! An excellent opportunity for Clinical Database Programmers at one of Europe's leading biometrics companies. This is an office-based role in Berlin. In this exciting role you will be providing technical expertise for the conduct of clinical trials across a broad range of therapy areas.
JOB TITLE:
Clinical Database Programmer / SAS Programmer / Programmer / Clinical Systems Programmer / Support Programmer
ROLE
*Provide technical expertise for the conduct of clinical trials to support various programming activities related to clinical systems within eClinical technologies.
*This role will involve both Database Programming and/or Clinical Systems & Support Programming depending on workload and experience
REQUIRED SKILLS
*Proficiency in at least one of the following programming languages : SAS, CDMS, EDC, SQL, VB, Java.
*Experience working with at least one system used in the clinical trial process (e.g. SAS, CDMS, EDC systems such as Inform, RAVE, Datalabs, CTMS etc.
*Clinical Trials/Pharmaceutical sector experience (including knowledge of ICH-GCP)
*Relevant degree
*Ability to learn new systems and function
LOCATION
Germany / Deutschland / Berlin
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, Samuel Stopp, on +44 (0)20 3189 0465, or email (url removed). If this role is not suitable, Samuel is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
SAS / Clinical Database Programmer / SAS Programmer / Programmer / Clinical Systems Programmer / Support Programmer / Germany / Deutschland / Berlin / SAS / CDMS / EDC / SQL / VB / Java / RAVE / Datalabs / CTMS
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Director of Programme Management – Respiratory, Late Phase |
| Location |
|
England, UK |
| Job Number |
|
120250077 |
| Posted |
|
08/02/2012 (18:30) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
JOB TITLE
Director of Programme Management - Respiratory, Late Phase
ROLE DESCRIPTION
An exciting role has opened up with a top 5 global CRO. This role would be ideal for a Project Director or Director of Project Management, who is looking to take the next career step into a more strategic role. The role available will involve driving the therapeutic strategy and growth of the Late Phase Respiratory Therapeutic Delivery Unit and therefore require a solid track record working on Respiratory studies. This position will be home based, and open to candidates in the UK, Spain, Germany, Netherlands, Italy and France.
REQUIREMENTS
*A Bachelor Degree in Life Science or related field, ideally a Masters or PhD.
*Extensive Project Management and Director Experience within a CRO is a MUST for this role.
*Experience within Respiratory Late Phase studies is desirable
*Good Negotiation techniques, and commercial and organizational acumen.
*Ability to lead, motivate and co-ordinate teams.
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:
Director/ Therapeutic Strategy Lead / 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 / The Netherlands /Europe / France / Spain /Respiratory / Late Phase
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Project Manager – (Respiratory LATE PHASE) Europe home |
| Location |
|
England, UK |
| Job Number |
|
120250075 |
| Posted |
|
08/02/2012 (18:10) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Clinical Project Manager - (Respiratory LATE PHASE) Europe home based
JOB SUMMARY
A Clinical Project Manager is required by a reputable and global Top 10 CRO to manage its Late Phase Respiratory 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 (Respiratory) / Clinical Project Leader
LOCATION
UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / London UK/ Poland / / Ireland / Spain / Belgium / France / Germany / 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 Internal Medicine including Respiratory 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 / 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 / London/ UK/
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Project Manager – CNS and Diabetes – London (Ph |
| Location |
|
England, UK |
| Job Number |
|
120250071 |
| Posted |
|
08/02/2012 (17:59) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Clinical Project Manager - CNS and Diabetes - London (Pharma)
JOB SUMMARY
A Clinical Project Manager is required for a global Pharmaceutical company to be based in Central London. You will be responsible for managing several studies within CNS, Diabetes and Anaemia. You will be primarily office based in their central London office, but there is some flexibility to work one day from home if required.
JOB TITLE
Clinical Project Manager / Project Manager / CNS / CPM/ PM /Clinical Study Manager / Diabetes/ Metabolic
LOCATION
UK/London / England
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 full-service domestic and international clinical studies
* Budget management, resource procurement and planning as well as project implementation.
* Client interactions -liaising with sponsor development updates and meetings, bid defence meetings.
*Participate in proposal development teams and represent at marketing and new business meetings.
* Mentoring junior staff and functional leads for specific projects.
REQUIREMENTS
A Life Science or Nursing Degree
Experience in clinical research, including previous CRA and Project Management Experience.
Experience in managing global studies particularly in CNS/or Diabetes
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 / London
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Biometrics Application Developer - London |
| Location |
|
London |
| Job Number |
|
120250068 |
| Posted |
|
08/02/2012 (17:52) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Biometrics Application Developer - London
This is a truly unique opportunity for an experienced Biometrician to join one of the world's leading Pharmaceutical Companies. Opportunities of this nature at a company of this stature don't come along often, so if you feel you have the necessary experience and ambition, then apply now. Calling all experienced Biometricians now!
JOB TITLE
Biometrics Application Developer - London
LOCATION
London
BENEFITS
Generous Salary
Opportunity for international travel
Extensive responsibility
ROLE/DESCRIPTION
Biometrics Standards & Technology is a global team creating innovative technological and process solutions for the Biometrics department. As part of our team your main tasks are:
* Provide statistical software and software development and documentation support to all groups within the Biometrics Department
* Develop and maintain analysis system tools and requirements with the user community
*Liaise with data managers, statisticians and statistical programmers working on early and/or development stage projects and participate in the lifecycle activities for generic tools (across project programs)
* Adapt quickly to a complex and dynamic technical environment
* Give advice and provide training on SAS and other software usage and support users in problem solving and business need analysis
* Provide input to process development and ensure compliance with group processes and overall company standards
* International travel 2-4 times per year
REQUIREMENTS
You're someone who wants to influence your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point. Education and Qualifications:
* University education or equivalent with major emphasis on numerate discipline and expert knowledge of SAS with UNIX and PC experience
* Significant experience in application development and in analysing clinical trials data in the pharmaceutical industry
* Ability to process information, analyse data, and reach conclusions based on sound reasoning
* Sound knowledge & understanding of industry data standards, in particular CDISC's SDTM and ADaM
* Expert understanding of safety analysis concepts for clinical trial data domains and advanced understanding of efficacy analysis concepts for clinical trials
* Ability to work in a global team and simultaneously on multiple activities
* Ability to communicate concisely, clearly and accurately in written reports and data, presentations and one-to-one meetings as required.
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
Biometrics / Application Developer / Head of Biometrics / Clinical Programming / Statistical Programming / Software Programming / SAS / Clinical / Data Management / Pharmaceutical Company / Pharmaceutical Industry / Switzerland / London / England
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Biometrics Application Developer - Basel |
| Location |
|
Basel, Non UK |
| Job Number |
|
120250067 |
| Posted |
|
08/02/2012 (17:48) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Biometrics Application Developer - Basel
This is a truly unique opportunity for an experienced Biometrician to join one of the world's leading Pharmaceutical Companies. Opportunities of this nature at a company of this stature don't come along often, so if you feel you have the necessary experience and ambition, then apply now. Calling all experienced Biometricians now!
JOB TITLE
Biometrics Application Developer - Basel
LOCATION
Basel
BENEFITS
Generous Salary
Opportunity for international travel
Extensive responsibility
ROLE/DESCRIPTION
Biometrics Standards & Technology is a global team creating innovative technological and process solutions for the Biometrics department. As part of our team your main tasks are:
* Provide statistical software and software development and documentation support to all groups within the Biometrics Department
* Develop and maintain analysis system tools and requirements with the user community
*Liaise with data managers, statisticians and statistical programmers working on early and/or development stage projects and participate in the lifecycle activities for generic tools (across project programs)
* Adapt quickly to a complex and dynamic technical environment
* Give advice and provide training on SAS and other software usage and support users in problem solving and business need analysis
* Provide input to process development and ensure compliance with group processes and overall company standards
* International travel 2-4 times per year
REQUIREMENTS
You're someone who wants to influence your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point. Education and Qualifications:
* University education or equivalent with major emphasis on numerate discipline and expert knowledge of SAS with UNIX and PC experience
* Significant experience in application development and in analysing clinical trials data in the pharmaceutical industry
* Ability to process information, analyse data, and reach conclusions based on sound reasoning
* Sound knowledge & understanding of industry data standards, in particular CDISC's SDTM and ADaM
* Expert understanding of safety analysis concepts for clinical trial data domains and advanced understanding of efficacy analysis concepts for clinical trials
* Ability to work in a global team and simultaneously on multiple activities
* Ability to communicate concisely, clearly and accurately in written reports and data, presentations and one-to-one meetings as required.
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
Biometrics / Application Developer / Head of Biometrics / Clinical Programming / Statistical Programming / Software Programming / SAS / Clinical / Data Management / Pharmaceutical Company / Pharmaceutical Industry / Switzerland / Basel
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Outsourcing and Vendor Management, Global Pharma |
| Location |
|
Buckinghamshire |
| Job Number |
|
120250035 |
| Posted |
|
08/02/2012 (16:07) |
| Agency/Employer |
|
i-Pharm Consulting |
| Description
|
|
Outsourcing and Vendor Management, Global Pharma
Outsourcing and Vendor Management required for a highly reputable and dynamic Pharmaceutical company based in Buckinghamshire. This is a permanent opportunity.
JOB TITLE
Outsourcing and Vendor Management / Outsourcing Manager / Vendor Management / Contracts Manager
LOCATION
UK / England / Buckinghamshire
BENEFITS
Generous Salary
Excellent on-going career development opportunities
ROLE/DESCRIPTION
- Support the evaluation, selection and management of service providers across R&D to ensure optimal selection and delivery of outsourced services
- Ensuring the appropriate use of various contractual agreements and tools (with Legal) and their tracking
- Ensuring appropriate archiving of clinical service documentation. Training obligations. Process improvement.
REQUIREMENTS
- At least 2 years of experience in CRO management and contract negotiation and/or as Business Development Manager within a CRO
- Project management experience at international level
- Business qualification and/or para-legal experience an advantage
- Life Science degree and/or clinical research experience an advantage
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
Outsourcing and Vendor Management / Outsourcing Manager / Vendor Management / Contracts Manager / UK / England / Buckinghamshire
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Project Manager – Late Phase (Respiratory) |
| Location |
|
England, UK |
| Job Number |
|
120249923 |
| Posted |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Senior Biostatistician - Berkshire |
| Location |
|
Berkshire |
| Job Number |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Clinical Quality Auditor, North West England |
| Location |
|
North West England, North West |
| Job Number |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Senior Biostatistician - Yorkshire, England |
| Location |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Associate Director,Regulatory Affairs/Study Start Up,SE England |
| Location |
|
England, UK |
| Job Number |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Regulatory Affairs Manager– Maidenhead, UK / home based – |
| Location |
|
South East England, South East |
| Job Number |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Senior Clinical Research Physician, North-West England |
| Location |
|
North West England, North West |
| Job Number |
|
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
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Senior Quality Assurance Auditor, home based |
| Location |
|
Berkshire |
| Job Number |
|
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)
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
