Associate Director, Pharmacovigilance
Background:
The Associate Director of Pharmacovigilance is responsible for assisting in the management and development of European safety management services. The successful candidate will ensure the delivery of safety management services consistent with company SOPs WPDs, ICH guidelines and regulatory requirements by working with Safety ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 12/25/2008 2:06:26 AM
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Clinical Research Associate
Background:
Our client is recruiting for a CRA to work for a Medical Devices company based in Germany. This position is field based where you will be managing studies across Germany and Switzerland. Please forward your CV in word format.
Additional Information: ... more
Type: Full Time Location: N/A Country: Germany Posted: 12/25/2008 2:06:25 AM
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REGULATORY PROJECT MANAGER **ONCOLOGY** CAMBRIDGE
Background:
We are currently working on a Regulatory Project Manager position focusing on Oncology products, and we are looking for someone who can work on these products from early development throught out the whole of the drug life cycle of the product.
Primary Duties: ... more
Type: Full Time Location: Cambridgeshire Country: East Anglia Posted: 12/25/2008 2:06:25 AM
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Clinical Research Associate II CRA - Global CRO! - Belgium
Background:
Paramount Clinical Research: Clinical Research Associate II CRA - Global CRO! - Belgium An international Clinical Research Organisation currently requires an ambitious Clinical Research Associate II CRA to join the team in Brussels, Belgium. The company is located in over 40 countries, ... more
Type: Full Time Location: N/A Country: Belgium Posted: 12/25/2008 2:06:25 AM
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Electrical Design Engineer
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Type: Full Time/Contract Location: N/A Country: United Kingdom Posted: 12/24/2008 2:10:24 AM
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Research Nurse
Background:
An excellent opportunity to join an internationally recognised CRO.
Primary Duties:
Primary role of the Research Nurse: • Provide support in set-up and implementation of the clinical phase of the study protocol in conjunction with ... more
Type: Full Time Location: Surrey, London, South/South East Country: Home Counties Posted: 12/24/2008 2:08:05 AM
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GMP Compliance Manager
Background:
My Client is looking for a Compliance Manager to join their team. For this position you will need to have experience in GMP Auditing and training.
Primary Duties:
The main duties of the role are: • Ensure the ... more
Type: Full Time Location: Buckinghamshire, Home Counties Country: Home Counties Posted: 12/24/2008 2:08:05 AM
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Clinical Trial Co-ordinator / CTC / Senior CTA required - PHARMA
Background:
My large and successful Pharma client is currently recruiting for a Clinical Trial Co-ordinator to closely assist the Clinical Team on large international studies.
Primary Duties:
I am looking for either an existing Clinical Trial Co-ordinator, or alternatively ... more
Type: Full Time Location: Middlesex, Home Counties Country: South/South East Posted: 12/24/2008 2:08:05 AM
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Scientific Advisor / Scientific Development / Onocology
Background:
• Global Biotechnology Leader • Impressive Portfolio • Flexible and supportive working environment • Growing Portfolio • Cash rich organisation with capacity to acquire/increase portfolio • Career Development Opportunities within Medical Affairs These MSL positions, within the ... more
Type: Full Time Location: Middlesex Country: South/South East Posted: 12/24/2008 2:08:04 AM
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Regulatory Affairs Manager
Background:
Growing specialist pharmaceutical company
Primary Duties:
• Maintenance of existing marketing authorisations. • Successful worldwide submissions for new marketing authorisations, variations, extension applications and line extension. • Good knowledge and appropriate interpretation of guidelines, directives etc. • Responsibility ... more
Type: Full Time Location: N/A Country: Switzerland Posted: 12/24/2008 2:08:04 AM
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CONTRACT PVG Data Entry Associate
Background:
My client is looking for a PVG Data Entry Associate for a 3 month contract role. The ideal candidate will possess similar experience. The role will involve entering PVG cases for a specific client. It will be office based, forty hours per week. Immediate start. ... more
Type: Contract Location: Hertfordshire Country: Home Counties Posted: 12/24/2008 2:08:04 AM
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Global Program Manager
Background:
My client is Global Pharma company looking for Program Manager. Candidates will require line management experience working on international trials. Applicants will also be expected to assist in the CRO / Vendor management for the company and ensure that the trials do not run over budget. ... more
Type: Full Time Location: N/A Country: Germany Posted: 12/24/2008 2:08:04 AM
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CONTRACT Lead Data Manager
Background:
My client is a large Pharmaceutical company requiring a Lead Data Manager on a 6 month contract. This role will be based full time on site for 40 hours per week. Tasks will include coordinating inhouse and outsourced clinical trials, as well as hands on ... more
Type: Contract Location: N/A Country: Belgium Posted: 12/24/2008 2:08:03 AM
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Contract Clinical Research Associate
Background:
My client is a Global Pharmaceutical Company. They are looking for a Clinical Research Associate to work on a initial 6 month contract. Main responsibilities will involve: • Site Initiation • Ethical Submissions • On site monitoring • Coordinating the ... more
Type: Contract Location: Berkshire Country: Home Counties Posted: 12/24/2008 2:08:03 AM
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Contract CRA - Netherlands
Background:
My Client is a Global Pharmaceutical Company they are looking for a Contract CRA to work on an initial 12 month contract. Your main responsibilities will be Selecting New sites within the Netherlands, Ethical Submissions, and Monitoring of sites across multiple therapy areas mainly Oncology ... more
Type: Contract Location: N/A Country: Netherlands Posted: 12/24/2008 2:08:03 AM
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Senior Clinical Research Associate / Senior CRA - Pharma
Background:
My large and successful Pharm client is looking for a Senior Clinical Research Associate / Senior CRA to work on a large Cardiovascular study.
Primary Duties:
I am currently searching, on behalf of my client, for a Senior ... more
Type: Full Time Location: Northern Ireland, UK Country: UK Posted: 12/24/2008 2:08:03 AM
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CONTRACT EU Pharmacovigilance Manager
Background:
My client is looking for an experienced Pharmacovigilance Manager for a 6 month contract in an EU focused role. Key responsibilities include ensuring compliance to pharmocovigilance legislation and contributing to the implementation of new or revised processes of the pharmacovigilance system. Knowledge of EU legislation and ... more
Type: Contract Location: Berkshire Country: Home Counties Posted: 12/24/2008 2:08:03 AM
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Regulatory Affairs Officer
Background:
Leading pharmaceutical company
Primary Duties:
• To provide full product life cycle regulatory support for OTC medicinal products, medical devices, food supplements and/or cosmetics as required by the UK and Ireland business needs. • Support the regulatory activities ... more
Type: Full Time Location: Buckinghamshire, Home Counties Country: Home Counties Posted: 12/24/2008 2:08:02 AM
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Regulatory Affairs Manager
Background:
Leading pharmaceutical company
Primary Duties:
• Manage and execute EMEA Regulatory activities within teams to meet Commercial/Regulatory requirements. • Develop regulatory strategies and formulate registration plans. • Co-ordinate Regulatory actions with European medical activities.• To manage EMEA Regulatory ... more
Type: Full Time Location: Berkshire, Home Counties Country: Home Counties Posted: 12/24/2008 2:08:02 AM
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PVG Physician
Background:
My client is based at a pharma in Berkshire. Your responsibilities will be to ensure accurate monitoring of the safety of products both during Phase I to IV clinical trials and after marketing authorisation approval. To be responsible for the preparation, review, approval and submission ... more
Type: Full Time Location: Berkshire Country: Home Counties Posted: 12/24/2008 2:08:02 AM
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