- Clinical Pharmacist
This is an exciting new position with a company who are expanding the team by recruiting registered pharmacists who are looking for a fresh challenge and change in direction.They are currently focused on increasing resource in London and The South East of England, The Midlands, The North West of England, The North East of England, Yorkshire and Scotland. ...
- PW 6590 Medical Science Liaison (MSL) Hepatitis C
Our client, a global healthcare leader is looking to recruit a Medical Science Liaison (MSL) to join its UK Medical Affairs Department focusing on its Hepatitis portfolio. The position, national in scope, will work alongside two other MSLs and two medical advisors playing a key role at this exciting time with an imminent launch.
- PW 6592 Medical Science Liaison (MSL) Antibiotics
Our client, a global healthcare leader, is looking to recruit a MSL to join its UK Medical Affairs Department to focus on its Antibiotics portfolio. The position, national in scope, will work alongside two other MSLs on a recent launch with another key launch likely later this year.
- PW 6579 Copy Reviewer / Medical Reviewer
Opportunity to join this dynamic and growing consultancy as a copy review expert. You’ll be passionate about improving the copy review process and part of an organisation changing copy review perceptions in the pharmaceutical industry. This really is an exciting opportunity to make a difference.
- CRA II / Senior CRA - London - Top 5 Pharma (via Global CRO) - Cardiovascular/Oncology Phase III
A Top 5 Pharmaceutical Company is looking for talented CRAs and Senior CRAs to support site-management activities in the London area, as part of a Global Phase III Oncology and/or Cardiovascular study.
The cutting-edge drugs involved in these trials have a great potential, the teams involved and investigators are highly enthusiastic in collaborating towards bringing the pipeline to life.
- CRA II / Senior CRA - Scotland - Top 5 Pharma (via Global CRO) - Cardiovascular/Oncology Phase III
A Top 5 Pharmaceutical Company is looking for talented CRAs and Senior CRAs to support site-management activities in the Scotland Territory area, as part of a Global Phase III Oncology and/or Cardiovascular study. The cutting-edge drugs involved in these trials have a great potential, the teams involved and investigators are highly enthusiastic in collaborating towards bringing the pipeline to life.
- Senior QA Associate/QA Associate – Leading Global Pharmaceutical firm – Belgium
My client, a leading global pharmaceutical firm are currently looking for an ambitious and driven individual to join them as a Senior QA Associate within their large and dynamic team. This company are keen to find long term employees keen on progressing and developing their careers.
- PW 6550 Senior Manager or Associate Director Global QA
This is an opportunity to take responsibility for ensuring high quality consistency of products in both development and commercial stages and contribute to QA support for commercial readiness activity. You will monitor the quality risk for QA of European marketed products in terms of GMP and GDP and well as coordinate Quality Assurance Activities with European manufacturing sites and EU Region Affiliates.
- Project Manager/ Clinical Consultant
A leading independent consultancy firm within the healthcare and life sciences industry are looking to appoint a Managing Consultant. The ideal candidate will have a proven track record of holding vendor management relationships, developing protocols and working with the world’s leading CROs and Pharmaceutical firms to create bespoke solutions to their data collection of clinical trials.
- UBC- Safety Scientist, Research & Clinical Services (Geneva)
FONT>Writing of procedural documents such as Adverse Event Reporting Plans (AERPs)Adverse Event case processing: receipt, data entry, coding, and evaluation of Adverse Event reports according to the applicable SOPs, including writing the narrative; perform seriousness, listedness and causality assessmentEnsure the quality and accuracy of data used to support any regulatory document, including but not limited to: ICSRs, aggregate data, requested line listingsAssist in the reconciliation of...