i-Pharm Consulting |
| Contact |
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| Telephone |
(0)20 3189 2299 |
| Email |
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| Website |
http://www.i-pharmconsulting.com |
| Address |
i-Pharm Consulting Ltd
, Grayton House
, 498 Fulham Road
, London
, SW6 5NH |
| Description |
The i–Pharm Healthcare Division is a leading supplier of staffing and consultancy services to the NHS and the private Healthcare Sector.
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). |
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| Job Title |
Senior Regulatory Affairs Specialist - Northwest |
| Salary/rate |
£40000 - £50000/annum FULL BENEFITS |
| Location |
Greater Manchester, Greater Manchester |
| Job Number |
120183762 |
| Posted |
19/03/2010 (10:55) |
| Agency/Employer |
i-Pharm Consulting |
Description
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Senior Regulatory Affairs Specialist – International Pharmaceutical Company – Northwest
SUMMARY
There is now the opportunity for an experienced senior Regulatory Affairs Specialist to join this international organisation in an exciting position where you will be responsible for getting to know their product range and dealing with all areas of this international business. This position will see you working very closely with their R&D team in a senior position.
JOB TITLE: Regulatory Affairs Specialist / RA Manager / Submissions Specialist
LOCATION: Northwest
COMPANY STATEMENT: This is an international pharmaceutical company who specialise in a number of market leading niche products. They have been growing continually and are at the forefront of their field. They are looking for bright, enthusiastic and innovative individuals who will grow and develop with the company.
SALARY: Attractive + Benefits
ROLE/DESCRIPTION: This is an exciting opportunity for an experienced Senior Regulatory Affairs Specialist to work in this brand new site within their New Product development NPD team. You will be required to manage the regulatory process ensuring all regulatory submissions, product licences, technical information and contracts are drafted, submitted and maintained in accordance with regulatory requirements. As a senior member of the team you will be combining knowledge of scientific, legal & business issues, as the crucial link between the company, its products and regulatory authorities, including the MHRS, FDA, EMEA and other markets throughout the world
REQUIREMENTS:
- Degree level education
- Experience in a similar environment
- Excellent Regulatory knowledge and experience both in Europe and the US
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. If this role is not suitable, Lauren 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, Senior Regulatory Affairs Specialist, RA, Submissions, MHRA, FDA, New Product Development, NPD
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| Job Type |
Contract |
| Contract Length |
12 MONTHS |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Regulatory Affairs RA Officer - Northwest |
| Salary/rate |
£25000 - £35000/annum FULL BENEFITS |
| Location |
Greater Manchester, Greater Manchester |
| Job Number |
120183759 |
| Posted |
19/03/2010 (10:32) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Regulatory Affairs Officer – International Manufacturing – Northwest
SUMMARY
There is now the opportunity for an experienced Regulatory Affairs Officer to join this international organisation in an exciting position where you will be responsible for getting to know their product range and dealing with all areas of this international business.
JOB TITLE: Regulatory Affairs Officer / RA Associate / Submissions Specialist
LOCATION: Northwest
COMPANY STATEMENT: This is an international pharmaceutical company who specialise in a number of market leading niche products. They have been growing continually and are at the forefront of their field. They are looking for bright, enthusiastic and innovative individuals who will grow and develop with the company.
SALARY: Attractive + Benefits
ROLE/DESCRIPTION: This is an exciting opportunity for an experienced RA Officer to work in this brand new site within their New Product development NPD team. You will be required to manage the regulatory process ensuring all regulatory submissions, product licences, technical information and contracts are drafted, submitted and maintained in accordance with regulatory requirements.
REQUIREMENTS:
- Degree level education
- Experience in a similar environment
- Excellent Regulatory knowledge and experience
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Regulatory Affairs, RA, Submissions, MHRA, FDA, New Product Development, NPD
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| Job Type |
Contract |
| Contract Length |
6 MONTHS |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Quality Assurance QA Officer GMP Northwest |
| Salary/rate |
£25000 - £35000/annum FULL BENEFITS |
| Location |
Greater Manchester, Greater Manchester |
| Job Number |
120183400 |
| Posted |
17/03/2010 (16:55) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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QA Officer / Quality Assurance Officer – International Manufacturing – Northwest
SUMMARY
There is now the opportunity for an experienced Quality Assurance Officer to join this international organisation in a senior position that will see you in a small team of experienced QA Officers reporting directly to the Head of Quality. This is an exciting and progressive company offering training and progression for all employees.
JOB TITLE: Quality Assurance Officer / QA Officer / GMP Associate
LOCATION: The North
COMPANY STATEMENT: This is an international pharmaceutical company who specialise in a number of market leading niche products. They have been growing continually and are at the forefront of their field. They are looking for bright, enthusiastic and innovative individuals who will grow and develop with the company.
SALARY: Attractive + SHIFT ALLOWANCE
ROLE/DESCRIPTION: This is an exciting opportunity for an experienced QA Officer to join an exceptionally friendly and supportive organisation in a new and state of the art sterile manufacturing facility.
- Implement and maintain quality standards
- Support manufacturing and other operation in the maintenance of cGMP
- Review and approve quality documentation
- Identify, design and deliver GMP training
- Review and approve batch manufacturing documentation for timely release
- Carry out audits and identify and correct any issues of non-compliance
REQUIREMENTS:
- Degree level education
- Experience in a similar environment (sterile manufacture)
- Excellent GMP knowledge
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Quality Assurance Officer, QA Officer, cGMP , GMP, Manufacturing, Sterile, manufacturing
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| Job Type |
Unknown |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
CLINICAL GLP STUDY DIRECTOR - PROJECT MANAGER |
| Salary/rate |
£25000 - £35000/annum FULL BENEFITS |
| Location |
South Yorkshire, South Yorkshire |
| Job Number |
120177915 |
| Posted |
16/03/2010 (12:52) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Study Director (GLP) Pre-Clinical CRO – Northeast – Salary Negotiable and Excellent benefits
SUMMARY
There is now the opportunity for an experienced Study Director to join this hugely successful organisation in a senior role within their UK operation. It is a strategically hands-on opportunity in their Quality assurance function and team and being the key point of contact for all Good Laboratory Practice GLP and knowledge.
JOB TITLE: Study Director / Project Manager / Good Laboratory Practice / GLP / cGLP / GCLP
LOCATION: York
COMPANY STATEMENT: Join an organisation that pride themselves on building strong relationships with their clients and aim to be regarded as an extension to their own development teams. When they commit to a deadline, clients can rest assured that it will be met, and that they will receive open and honest feedback from their scientists where problems are met with an honest, proactive approach and with sponsors being informed every step of the way. This is a highly respected organisation who are looking for a professional and enthusiastic individual to join them now.
BENEFITS: Salary, pension, private healthcare, training, parking.
ROLE/DESCRIPTION: This is an exciting opportunity for a Pre-Clinical Study Director. You will be responsible for the direction of bioanalytical studies in a GLP environment and leading of all members of the team. Experience in LC/MS/MS and method development would be a distinct advantage.
Required:
- Degree level education (or equivalent)
- Excellent GLP knowledge and experienced Study Director
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Study Director, Project Management, Pre-Clinical, GLP, Good Laboratory Practice
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
QUALITY ASSURANCE AUDITOR - LABORATORY AUDITOR GLP GCLP |
| Salary/rate |
£20000 - £30000/annum FULL BENEFITS |
| Location |
South Yorkshire, South Yorkshire |
| Job Number |
120180498 |
| Posted |
16/03/2010 (12:47) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Clinical Quality Assurance Auditor GCP GLP GCLP – CRO - Excellent benefits and Progression
SUMMARY
There is now the opportunity for an experienced Quality Auditor to join this hugely successful organisation in a senior role within their UK operation. It is a strategically hands-on opportunity in their Quality assurance function and team and being the key point of contact for all Good Clinical Practice GCP knowledge and expertise as well as Good Laboratory Practice GLP.
JOB TITLE: Clinical Quality Assurance Auditor / Clinical QA Auditor / GCP Auditor / GCP / cGCP / Good Clinical Practice / Good Laboratory Practice / GLP / cGLP / GCLP
LOCATION: York
COMPANY STATEMENT: Join an organisation that pride themselves on building strong relationships with their clients and aim to be regarded as an extension to their own development teams. When they commit to a deadline, clients can rest assured that it will be met, and that they will receive open and honest feedback from their scientists where problems are met with an honest, proactive approach and with sponsors being informed every step of the way. This is a highly respected organisation who are looking for a professional and enthusiastic individual to join them now.
BENEFITS: Salary, pension, private healthcare, training, parking.
ROLE/DESCRIPTION: This is an exciting opportunity for a Quality Assurance Auditor. You will be evaluating non-conformities and report findings. You will be consulting with other staff members for interpretation of regulations and performing regulatory compliance reviews for new and updated the company’s SOPs.
You will undertake independent Good Laboratory Practice (GLP) of work conducted in the company's bioanalytical laboratory facilities as required by regulatory guidelines. They will also be responsible for undertaking Good Clinical Practice (GCP) monitoring of bioanalytical analysis in support of clinical trials.
Required:
- Degree level education (or equivalent)
- Excellent GCP knowledge and experienced auditor
- Excellent GLP knowledge and experience
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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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Quality Assurance Auditor, Clinical QA Auditor, QMS, Quality Management System, Quality Systems Manager, GCP, cGCP, GCP Auditor, Audits, Auditing
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
QUALITY ASSURANCE MANAGER AND QUALIFIED PERSON QP |
| Salary/rate |
£40000 - £55000/annum FULL BENEFITS |
| Location |
Greater Manchester, Greater Manchester |
| Job Number |
120182047 |
| Posted |
16/03/2010 (11:53) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Quality Assurance Manager and Qualified Person QP – National Pharmaceutical Manufacturing - £50,000 + Excellent benefits - Northwest
SUMMARY
There is now the opportunity for an experienced Quality Assurance Manager to join this hugely successful organisation in a very senior role within their UK operation. It is a strategically hands-on opportunity dealing with their entire quality system.
JOB TITLE: Quality Assurance Manager / Quality Systems Manager / QA Manager / Qualified Person / QP
LOCATION: Northwest
COMPANY STATEMENT: They are a national organisation with an impressive repertoire of clients for whom the manufacture a wide range of leading pharmaceutical products from solid oral dose to inhalers. The manufacture large scale both for commercial release and clinical trials.
BENEFITS: Salary, pension, very competitive bonus, private healthcare, training, parking.
ROLE/DESCRIPTION: This is an exciting opportunity for a Quality Assurance Manager and Qualified Person (QP). You will be responsible for leading the QA and documentation functions for the site, the release of Investigational Medicinal Products (IMPs) and for the progression of the company and systems with regards to GMP.
Requirements:
- Prior experience of Quality System Management
- Excellent cGMP knowledge
- Registered QP (IMPs)
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. 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
Quality Assurance Manager, QA Manager, QMS, Quality Management System, Quality Systems Manager, GMP, cGMP, Qualified Person, QP
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
CONTRACT QUALIFIED PERSON QP - NORTHWEST |
| Salary/rate |
£400 - £600/day |
| Location |
Greater Manchester, Greater Manchester |
| Job Number |
120183328 |
| Posted |
15/03/2010 (15:47) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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6 MONTH CONTRACT QA Manager & Qualified Person – Pharmaceutical Manufacturing – Northwest
This Contract Manufacturing Organisation now requires an experience QA manager and Qualified Person QP to step in and oversee the compliance of the release of their sterile products.
JOB TITLE: QA Manager / QP / Qualified Person / Quality Assurance Compliance Manager
BACKGROUND: This opportunity is for an experienced Qualified Person to join this contract manufacturing organisation releasing their active pharmaceutical ingredients in solid dosage format in a sterile environment. This role requires prior batch release experience and of course excellent GMP experience. You will be required to be named on their licence.
ROLE: Contract/Interim/Locum/ Consultant QA Manager & Qualified Person
EXPERIENCE REQUIRED: QA Management, registered QP, release of steriles, man management.
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Lauren Bell-Misri on +44 (0)20 3189 2299, or email lbell-misri@i-pharmconsulting.com. If this role is not suitable, Sarah 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, Regulatory & 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
Quality Assurance QA Manager, Compliance, Qualified Person, Quality Assurance, Batch Release, Good Manufacturing Practice, GMP, API
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| Job Type |
Contract |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coding, Essex |
| Salary/rate |
£275 - £350/day |
| Location |
Essex, Essex |
| Job Number |
113424804 |
| Posted |
15/03/2010 (11:34) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Our NHS Client is based in Essex and they require a high calibre contract Clinical Coder to join their centralised team as soon as possible. Our client is willing to offer a 6 month position as long as the applicant can prove their capability to achieve high output (30-40 case notes per day depending on casemix) and accuracy across most specialities.
Clinical Coders applying to this advert musty have completed a foundation course in Clinical Coding at least 3 years ago and preferably you will also hold the National Clinical Coding Qualification (NCCQ/ ACC).
i-Pharm Healthcare provides free of charge training to all of its Clinical Coders in the form of Refresher Courses (both bespoke and Connecting for Health), Speciality Workshops, and ACC Revision Workshops. We can also offer these courses to external contractors at a charge.
We welcome calls to discuss this Clinical Coding opportunity and all applications are treated in the strictest confidence.
Skills:
+ ACC qualification preferred
+ Must have significant experience of coding background in an NHS Hospital environment.
+ Knowledge of ICD10 and OPCS4 are essential.
+ Competent in coding all specialities.
+Able to commute daily to Essex.
+ Full time position working 37.5 hours per week.
+ References will be checked prior to being put forward to this Trust.
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| Job Type |
Contract |
| Contract Length |
6 Months |
| Start Date |
22/3/2010 or AS |
| Contact Details |
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| Job Title |
Drug Safety Coordinator - drug safety - Thames Valley |
| Salary/rate |
£20000 - £21000/annum |
| Location |
Wiltshire, Wiltshire |
| Job Number |
120183249 |
| Posted |
12/03/2010 (18:23) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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COMPANY:
Pharmaceutical with medium sized team and a small drug safety function. recently have purchased a number of new products and the safety team will be going through a period of growth. This 6 month contract is likely to be extended given the volume of the work.
The role:
You will provide support to the medical director and the other members of the drug safety team within all aspects of drug safety. This is a good role for an associate to gather some more experience within a recognised pharmaceutical company.
Experience:
Ideally you will be either an experienced drug safety administrator or a junior drug safety associate looking to gain some further experience and exposure to the industry.
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Consultant David Hendron on +44 (0)20 3189 2299, or email dhendron@i-pharmconsulting.com. If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Clinical Project Manager, Late Phase, London |
| Location |
City of London, London |
| Job Number |
120181958 |
| Posted |
11/03/2010 (19:10) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Clinical Project Manager, Late Phase, London
SUMMARY
Clinical Project Manager / Project Manager required by established International CRO as part of their ongoing expansion into Europe. The role is based from the company’s European HQ in London or can be home-based. You will be project managing international clinical trials in Phase IIIb/IV across multiple therapy areas.
JOB TITLE
Clinical Project Manager / Project Manager / Clinical Study Manager / Late Phase / Phase IIIb/IV
LOCATION
UK, South-East, South East, SE, London
COMPANY STATEMENT
You will be joining an established International mid-sized CRO who are expanding ther global presence through growth in Europe. The company place particular emphasis on the post marketing / approvals area specialising in Phase IIIb / IV Clinical Trials.
BENEFITS
Generous Salary
Car Allowance
Bonus
Pension
Life Assurance
Private Healthcare
Excellent ongoing career development opportunities
ROLE/DESCRIPTION
You will be Project Managing International Clinical Trials in Phase IIIb-IV across a range of therapeutic areas.
REQUIREMENTS
Life sciences degree OR nursing qualification
5+ years experience in Clinical Research
2+ years Clinical Project Management experience
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Stephen McAnaney on +44 (0)20 3189 2299, or email smcananey@i-pharmconsulting.com. 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
Clinical Project Manager, Project Manager, Senior Clinical Project Manager, Clinical Project Director, Clinical Study Manager, Clinical Research Manager, UK, South-East, SE, London
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Associate Director of Project Management, Late Phase |
| Location |
England, UK |
| Job Number |
120181260 |
| Posted |
11/03/2010 (19:10) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Associate Director of Project Management, Late Phase
SUMMARY
Associate Director of Project Management (Late Phase Clinical Research) required by International CRO. Applicants will be experienced Senior Clinical Project Managers or Project Directors and must have significant experience managing Late Phase / Phase IV Clinical Trials. This role can be based from the office or from home (UK, Germany, France).
JOB TITLE
Associate Director of Project Management, Late Phase / Senior Clinical Project Manager / Project Director
LOCATION
UK, England, Scotland, Germany, France
COMPANY STATEMENT
You will be working for one of the foremost Global CROs. The company works with the majority of Top Global Pharmaceutical Companies and has projects ongoing in therapy areas that include Oncology, Cardiovascular, Infectious Disease, CNS and Diabetes.
BENEFITS
Competitive Salary
Car Allowance
Pension
Private Healthcare
Life Assurance
Flexible working arrangements
Welcoming and inclusive company culture
ROLE/DESCRIPTION
You will be responsible for managing International Full-Service Projects in Late Phase (Phase IIIb/IV) Clinical Research across a range of therapeutic areas.
You will be the primary point of contact with the sponsor and will have overall responsibility for budgets and timelines.
REQUIREMENTS
10yrs Clinical Research experience
Significant full service Clinical Project Management and specific Late Phase (Phase IIIb/IV) Project Management experience
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Stephen McAnaney on +44 (0)20 3189 2299, or email smcananey@i-pharmconsulting.com. 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
Clinical Project Manager, Senior Clinical Project Manager, Clinical Project Director, Associate Director Project Management, Late Phase, Phase IIIb, Phase IV, Post Marketing, Approvals, Registry
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coder, 1 Month |
| Salary/rate |
£300 - £350/day |
| Location |
London, London |
| Job Number |
113424384 |
| Posted |
11/03/2010 (11:27) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Our Client is a NHS Hospital Trust based in South East London They are seeking two ACC qualified Clinical Coders who can join the existing centralised Clinical Coding Team for a period of 1 month to assist with annual leave staff shortages. This is an excellent opportunity for a permanent Clinical Coder to sample the contract market or alternatively it could serve to fill the gap between two longer contracts.
Our client hopes to find contract Clinical Coders who also hold the National Clinical Coding Qualification (NCCQ/ACC) so that their high standards can be maintained and deadlines can be met. However they will consider a Clinical Coder who can demonstrate extensive OPCS4.4/4.5 and ICD10 knowledge coupled with up to date Clinical Coding Training and Development. It may be necessary to test this at interview.
i-Pharm Healthcare provides free of charge training to all of its Clinical Coders in the form of Refresher Courses (both bespoke and Connecting for Health), Speciality Workshops, and ACC Revision Workshops. We can also offer these courses to external contractors at a charge.
Ideally applicants will have:
:- The ACC
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
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| Job Type |
Contract |
| Contract Length |
1 Month - Annua |
| Start Date |
6/4/2010 |
| Contact Details |
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| Job Title |
Clincial Coder - Imemdiate Start - Central London |
| Salary/rate |
£300 - £350/day |
| Location |
South East England, South East |
| Job Number |
113424217 |
| Posted |
10/03/2010 (12:49) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Our client urgently requires a Clinical Coder to work on a whole range of their medical records .
This is an urgent requirement offering an immediate start to suitable a Clinical Coder(s). The salary will be awarded dependant on experience. Our client recignises that experience as well as the ACC are important and an emphasis is placed upon relevant Clinical Coding experience to date.
Therefore ACC is not essential but solid and demonstrable Clinical Coding experience is. Successful applicants will be able to take advantage of i-Pharm's complimentary training packages including annual Clinical Coding Refresher Courses and speciality workshops.
Ideally applicants will have:
:- The ACC
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
Please contact Colin Lynam or Richard Gibson for further information on 0203 189 2299 and send your CV via this advert.
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| Job Type |
Contract |
| Contract Length |
3 Months |
| Start Date |
22/2/2010 or AS |
| Contact Details |
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| Job Title |
Lead CRA, Late Phase, Geneva / Switzerland |
| Location |
Switzerland, Non UK |
| Job Number |
120182871 |
| Posted |
10/03/2010 (09:13) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Lead CRA, Late Phase, Geneva / Switzerland
SUMMARY
Lead CRA required by specialist CRO based in Geneva, Switzerland. As a Lead CRA you wil be responsible for overseeing CRAs working on assigned Late Phase projects.
You will have significant experience of Late Phase Clinical Research (IIIb/IV) and will have the opportunity to work on an exciting range of projects including peri-approval studies, outcomes research, post marketing, registry studies, safety surveillance and risk management.
Superb salary packages and career development opportunities are on offer for talented Senior or Lead CRAs.
JOB TITLE
Lead CRA / Clinical Lead / LCRA / Senior CRA / SCRA
LOCATION
Switzerland, Geneva, Lake Geneva, Lausanne
COMPANY STATEMENT
You will be joining a specialist and rapidly expanding CRO with offices in North America and Europe.
BENEFITS
Generous salary CHF
Full benefits package
Excellent career development opportunity with expanding international company
Fantastic quality of life in Lake Geneva area
ROLE/DESCRIPTION
As Lead CRA you will also oversee study start-up activities, including site selection and regulatory document collection, development of monitoring plans and study templates and during study operations you will be responsible for reviewing monitoring visit reports and ensuring CRA adherence to study timelines and budget. You will also present at and participate in Investigator Meetings, other study trainings and meetings as required and act as a mentor for more junior Clinical Research Associates.
REQUIREMENTS
Life Sciences Degree OR Nursing Qualification
Previous experience of Late Phase Clinical Research
Previous experience as a Senior OR Lead CRA
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Stephen McAnaney on +44 (0)20 3189 2299, or email smcananey@i-pharmconsulting.com. 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
Lead CRA, Clinical Lead, Senior CRA, LCRA, SCRA, Late Phase, Phase IIIb, Phase IV, Peri-Approvals, Post Marketing, Registry, Patient Registries, Switzerland, Suisse, Svizzera, Geneva
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coding, NW London, ACC |
| Salary/rate |
£275 - £300/day |
| Location |
London, London |
| Job Number |
113424167 |
| Posted |
10/03/2010 (09:11) |
| Agency/Employer |
i-Pharm Consulting |
| Description
|
Clinical Coder - 6 Month Initial Contract - North West London
Our Client in an NHS Trust based in North West London. They are urgently seeking to increase their contract headcount in order to maximise their current output. This is a 6 month contract which will extend as long the Clinical Coding work is seen to be of high quality and the Clinical Coder can cover a range of specialities whilst maintaining high accuracy and working to National Standards.
i-Pharm works closely with its Clinical Coders and individuals taking up this position (or any other coding position currently advertised) will have an opportunity to avail of i-Pharm's 4 day Clinical Coding Refresher courses and speciality workshops.
Ideally these Clinical Coders will have:
:- The ACC (preferred but not essential)
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
We welcome anyone with queries to get in touch for an informal chat. All conversations are treated with the strictest of confidence.
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| Job Type |
Contract |
| Contract Length |
6 Months |
| Start Date |
15/3/2010 or AS |
| Contact Details |
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| Job Title |
Drug Safety / pharmakovigilanz Manager – drug safety |
| Salary/rate |
£40414 - £53886/annum |
| Location |
Köln, Non UK |
| Job Number |
120182852 |
| Posted |
09/03/2010 (17:41) |
| Agency/Employer |
i-Pharm Consulting |
| Description
|
COMPANY STATEMENT
This is a medium sized company with a friendly and good culture based on achieving great results through great individuals working in great teams. They are currently going through a very strong growth period following increase in sales from successful products. The drug safety /pharmakovigilanz department is expected to grow over the next ½ years and the drug safety quality manager is an important part of their successful growth.
BENEFITS
Fantastic basic salary and an appealing benefits package are on offer to the successful candidate
ROLE/DESCRIPTION
Development of and management of standards within drug safety function (SOPs)
Monitor and ensure compliance with regulatory laws and guidance
Work with internal colleagues to evaluate and improve compliance standards of pharmakovigilanz department.
Training of safety staff on compliance issues and standards.
REQUIREMENTS
You will need good previous drug safety / pharmakovigilanz experience
It will be good if you have previous experience in compliance or quality position
It will be good if you have previous experience or pharmakovigilanz audits or inspections
You will need to speak good English, other languages would be a bonus
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Consultant David Hendron on +44 (0)20 3189 2299, or email dhendron@i-pharmconsulting.com. If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
Drug safety, pharmacovigilance, drug safety officer, pharmacovigilance officer, drug safety associate, pharmacovigilance associate, drug safety manager, pharmacovigilance manager, PSUR, PV, ASR, clinical safety, drug safety jobs, pharmacovigilance jobs. Pharmakovigilanz, pharmakovigilanz manager, pharmackovigilanz specialist
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
ASAP |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coding. Band 5 |
| Salary/rate |
£20000 - £27000/annum |
| Location |
Essex, Essex |
| Job Number |
121139992 |
| Posted |
08/03/2010 (16:23) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Our Client is a large NHS Foundation Trust in North East Essex. They are seeking to recruit at least one experienced and/or qualified Clinical Coder (ACC/ NCCQ) to join their Clinical Coding Team. You will be responsible for the abstraction of clinical data from patient records and translating it into diagnostic (ICD10) and procedural (OPCS4.5) coding classifications.
Suitable candidates will be ACC Qualified or working towards this qualification. To meet the requirements of a Band 5 you will need to be flexible in your approach and able to work as part of a team to tight deadlines. You will have a good knowledge of medical terminology, anatomy and physiology.
Suitable candidates will also be able to demonstrate competence in the use of ICD10 and OPCS 4.5 classifications, complete coding rules and the application of national clinical coding standards across acute specialities.
Candidates who currently do not meet the requirements of a band 5 may be considered for a development role at band 4 as long as the Clinical Coding Foundation Course has been completed. This will progress to a band 5 once relevant experience is gained or ACC examination has been passed
Ideally applications will have:
:- The ACC
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
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| Job Type |
Permanent |
| Contract Length |
N/A |
| Start Date |
26/4/2010 or AS |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coding |
| Salary/rate |
£250 - £350/day |
| Location |
East London, London |
| Job Number |
113423760 |
| Posted |
08/03/2010 (13:01) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Clinical Coder - 3 Months Rolling Contract - Extension likely
Our centrally located London NHS Trust requires two additional Clinical Coders to maximise their current output. This is a 3 month rolling contract which will extend as long the Clinical Coding work is seen to be of high quality and the Clinical Coder can cover a range of specialities whilst maintaining high accuracy and working to National Standards.
i-Pharm works closely with its Clinical Coders and individuals taking up this position (or any other coding position currently advertised) will have an opportunity to avail of i-Pharm's 4 day Clinical Coding Refresher courses and speciality workshops.
Ideally these Clinical Coders will have:
:- The ACC (preferred but not essential)
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
We welcome anyone with queries to get in touch for an informal chat. All conversations are treated with the strictest of confidence.
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| Job Type |
Contract |
| Contract Length |
3 Months |
| Start Date |
15/3/2010 |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coding, Contract |
| Salary/rate |
£250 - £280/day |
| Location |
South West London, London |
| Job Number |
113423756 |
| Posted |
08/03/2010 (12:38) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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**URGENT REQUIREMENT: INTERVIEWS THIS WEEK - APPLY IMMEDIATELY. As we are out of the office please email cv's/ queries to clynam@i-pharmconsulting.com
Contract Clinical Coder sought for an immediate start on a 6 month contract with our London based NHS Client.This well located NHS Trust requires additional headcount to maximise their current output. Our client always insists on high quality clinical coders you can display accurate and timely clinical coding abilities during interview.
i-Pharm works closely with its contractors and Clinical Coders taking up this position (or any other coding position currently advertised) will have an opportunity to avail of i-Pharm's Clinical Coding Refresher courses and bespoke training,.
Ideally applicants will have:
:- The ACC (not essential)
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
We welcome anyone with queries to get in touch for an informal chat. All conversations are treated with the strictest of confidence.
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| Job Type |
Contract |
| Contract Length |
6 Months |
| Start Date |
15/3/2010 or AS |
| Contact Details |
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| Job Title |
Clinical Coder, Clinical Coding |
| Salary/rate |
£275 - £3350/day |
| Location |
London, London |
| Job Number |
113423753 |
| Posted |
08/03/2010 (12:32) |
| Agency/Employer |
i-Pharm Consulting |
| Description
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Clinical Coder - 3 Months Rolling Contract - Extension
Our centrally located NHS Trust requires two additional Clinical Coders to maximise their current output. This is a 3 month rolling contract which will extend as long the Clinical Coding work is seen to be of high quality and the Clinical Coder can cover a range of specialities whilst maintaining high accuracy and working to National Standards.
i-Pharm works closely with its Clinical Coders and individuals taking up this position (or any other coding position currently advertised) will have an opportunity to avail of i-Pharm's 4 day Clinical Coding Refresher courses and speciality workshops.
Ideally these Clinical Coders will have:
:- The ACC (preferred but not essential)
:- In-depth OPCS4.5 and ICD10 knowledge and awareness
:- Broad case mix exposure
:- High levels of accuracy and output
:- An ability to cope with coding from different sources
:- An ability to code using varied technological mediums.
We welcome anyone with queries to get in touch for an informal chat. All conversations are treated with the strictest of confidence.
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| Job Type |
Contract |
| Contract Length |
3 to 6 Months |
| Start Date |
15 March 2010 o |
| Contact Details |
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