Clinical Research Associate
Background:
An excellent opportunity for an experienced CRA to join an established and busy CRO based in Buckinghamshire. Your responsibilities will include pre selection, initiation, monitoring and close out of study centres. This role will also include the opportunity to work with international clinical trials. ... more
Type: Full Time Location: Buckinghamshire, Home Counties Country: Home Counties Posted: 11/13/2008 1:36:39 AM
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Senior Clinical Trial Head
Background:
Accountable for all aspects of assigned Cardiovascular clinical trials including leading Clinical Trial Team s . Number of clinical trials depends on the workload and complexity of the individual trials. Responsible for program level activities as assigned. 1. Independently translate the Clinical ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/13/2008 1:36:39 AM
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Clinical QA Auditor/ GCP Auditor
Background:
Our client is a highly innovative, CRO which offers intelligent global clinical solutions, specifically designed to meet the individual needs of pharmaceutical and biotech sponsors. With a presence across all major continents, including emerging regions such as Asia Pacific, they provide services in clinical monitoring, ... more
Type: Full Time Location: Buckinghamshire, Home Counties Country: Home Counties Posted: 11/13/2008 1:36:38 AM
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Clincial Scientist
Background:
Our Client a TOP 20 Pharmaceutical company with a wide range of products are now looking to recruit a Clinical Scientist. The purpose of this role is to effectively plan , manage and execute assigned clinical trials to ensure that timelines, budget, and quality standards ... more
Type: Full Time Location: Berkshire, London, Home Counties Country: Home Counties Posted: 11/13/2008 1:36:38 AM
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Head of Regulatory Affairs / Head of Site / Senior Regulatory Affairs Manager
Background:
This position is to Head the Regulatory Division of a well known Pharmaceutical Company’s manufacturing site. You’ll provide full regulatory support to the company, in order to obtain and maintain Marketing and Manufacturing Authorisations for commercial products in the EU, USA and other ... more
Type: Full Time Location: Manchester, North West Country: Midlands Posted: 11/13/2008 1:36:38 AM
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Sr. Compensation and Benefits Manager
Responsibilities
Develops and implements the C&B strategy, policies and processes for GEHC. The role also contributes to the development of GE-wide C&B policies, working with the GE Corporate C&B Team and, in particular, manages the relationship with Corporate regarding GEHC's Executive Reward. The role is ... more
Type: Full Time/Contract Location: London Country: United Kingdom Posted: 11/12/2008 1:39:12 AM
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FIELD BASED PROJECT MANAGER (Registry Manager UK
Background:
My Client wishes to set up and run a UK registry for patients being prescribed one of their recently approved drugs. This is in the area of cancer pain and the product will only be prescribed by hospital physicians. The registry is intended to ... more
Type: Full Time Location: England Country: UK Posted: 11/12/2008 1:33:05 AM
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CTA - CLINICAL TRIAL ASSISTANT
Background:
CTA Clinical Trial Administrator Pharma CRO Excellent opportunity Spain/Madrid
Primary Duties:
I have a new role for a CTA-Clinical Trial Administrator. Candidates must have at least 6 months previous experience as ... more
Type: Full Time Location: N/A Country: Spain Posted: 11/12/2008 1:33:05 AM
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CRO Lab Manager
Background:
1. Lead the CRO Central Lab Reference Lab and Speciality provider selection process on a study-by-study basis under guidance and supervision of Local Head 2. Deliver excellent value for the company cost savings, cost reductions whenever possible 3. Assist Clinical Teams ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/12/2008 1:33:05 AM
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Key Account Manager Haematology - Wanted in South
Background:
A challenging opportunity has arisen for motivated and enthusiastic individual to join a global biopharmaceutical company committed to clinical accomplishment and patient support. This fantastic role is required for South of England.
Primary Duties:
This is a challenging brand new role ... more
Type: Full Time Location: Surrey Country: Home Counties Posted: 11/12/2008 1:33:05 AM
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Senior Statistical Programmer
Background:
You will be responsible for all programming aspects analysis datasets, pooled datasets, listings and tables of individual Phase I-IV clinical trials as well as project level activities for small drug project indications. You will have access to a large international ... more
Type: Full Time Location: N/A Country: Switzerland Posted: 11/12/2008 1:33:04 AM
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Global Studies Manager
Background:
CTC Clinical Trial Consulting, founded in Basel, Switzerland in 1997, is a specialist staffing organisation, providing flexible resourcing solutions to the pharmaceutical industry in Switzerland, with contract and permanent placements in clinical development, data management, statistics, regulatory affairs and medical marketing. For one ... more
Type: Contract Location: N/A Country: Switzerland Posted: 11/12/2008 1:33:04 AM
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Clinical Research Associates/Monitors
Background:
CTC Clinical Trial Consulting, founded in Basel, Switzerland in 1997, is a specialist staffing organisation, providing flexible resourcing solutions to the Swiss pharmaceutical industry in Switzerland, with contract and permanent placements in clinical development, data management, statistics, regulatory affairs and medical marketing. For ... more
Type: Contract Location: N/A Country: Switzerland Posted: 11/12/2008 1:33:04 AM
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Pharmacovigilance Officer
Background:
Pharmaceutical Company
Primary Duties:
You will contribute to the monitoring of the safety of the Group’s products, both during development and after marketing authorisation approval, in order to meet international regulatory requirements, the Company’s development objectives and ... more
Type: Full Time Location: Berkshire Country: Home Counties Posted: 11/12/2008 1:33:04 AM
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Clinical Operations Manager
Background:
Our client is recruiting for a Clinical Operations Manager to work for a Pharmaceutical company based in The Netherlands. Ideally you will have experience in managing clinical projects mainly in Phase II and III clinical trials. Please forward your CV in word format.
... more
Type: Full Time Location: N/A Country: Netherlands Posted: 11/12/2008 1:33:03 AM
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CRO Lab Manager
Background:
1. Lead the CRO Central Lab Reference Lab and Speciality provider selection process on a study-by-study basis under guidance and supervision of Local Head 2. Deliver excellent value for the company cost savings, cost reductions whenever possible 3. Assist Clinical Teams ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/12/2008 1:33:03 AM
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Senior Regulatory Affairs Associate – Project Manager
Background:
Regulatory Affairs with commercial focus Excellent Package Sydney based A dynamic Senior Regulatory Affairs role which requires business focus and client interaction while working across all areas of Regulatory Affairs. Our client is a major Consultancy in ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/12/2008 1:33:03 AM
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Lead Drug Safety Physician
Background:
Leading international pharmaceutical company
Primary Duties:
Duties will include pharmacovigilance monitoring responsibilities across the complete lifecycle of products within the oncology area. This will include carrying out signal detection activities and evaluating safety information from post marketing and ... more
Type: Full Time Location: N/A Country: Switzerland Posted: 11/12/2008 1:33:02 AM
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Full or Part-time Clinical Research Physicians
Background:
Are you looking for an exciting new career in the Pharmaceutical Industry? Do you have at least two year’s surgical experience? Can you work to tight timelines producing excellent high quality results? If so, you may be the person we are looking ... more
Type: Full Time Location: North Yorkshire, North East Country: North East Posted: 11/12/2008 1:33:02 AM
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Medical Devices - Quality and Regulatory Specialist
Background:
Medical Devices - Quality and Regulatory Specialist Berkshire £37K A major Medical Devices Company requires a Quality and Regulatory Specialist to be responsible to ensure that the (Devices) Quality Systems conforms with all reference standards and regulatory requirements (ISO 13485, ... more
Type: Full Time Location: Berkshire Country: Home Counties Posted: 11/12/2008 1:33:02 AM
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