- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging Markets
My client, a leading Biotech company, with a global presence and highly reputable market presence, is looking for a Manager within their Regulatory Team. This company is rapidly growing year on year and producing products that are changing the world. With more and more MA applications happening each year, their expansion is set to continue exponentially. ...
- Associate Director Regulatory Affairs
Associate Director, Regulatory Affairs - Cambridgeshire
A lot of regulatory professionals will be lucky if they get within touching distance of a MAA in a 4/5 year period. My client is expecting to push 1 or 2 out a year. Be part of something big and help it become even bigger!
My client, a leading Biotech company with global coverage and highly reputable market presence, is looking for a Manager within their Pharmacovigilance team. ...
- Senior Regulatory Affairs Specialist
We are recruiting for a Senior Regulatory Affairs Specialist for a permanent contract with a global pharma company. Competitive salary offered.
- Regulatory Affairs Specialist
We are recruiting for a Regulatory Affairs Specialist for our client in Berkshire offering a competitive salary.
- Pharmacovigilance Project Manager
An exciting opportunity has arisen with a market leading CRO who are actively looking for a Pharmacovigilance Project Manager. This opportunity would best suit someone with extensive experience within Drug Safety and who are looking to take that next step in an organisation which is experiencing rapid but sustainable growth.
- Senior Pharmacovigilance Scientist
Brand new Senior Pharmacovigilance Scientist opportunity with a leading pharmaceutical company!
Senior Pharmacovigilance Scientist
Location: Alderley Park, Cheshire
6 month contract with competitive daily rate or opportunity to be permanently employed by Clinical Professionals with attractive salary and benefits package
Offers exposure to early phase and oncology studies
- Pharmacovigilance Scientist -6 month contract
Pharmacovigilance Scientist -6 month contract with Strong chance of extension depending on Clinical trial results
We are currently working with a Top 20 Pharma company with one of the strongest drug pipelines in the industry to source a Global Pharmacovigilance Scientist for a new set of Clinical trials.
- Senior Regulatory Affairs Manager, England
My client is a leading research-based global pharmaceutical company, and they focus on the discovery, development, manufacturing and marketing of a large variety of top-quality pharmaceutical products. They have recently created this role in London for an experienced senior manager to join their team in order to sustain compliance and aid the company's Marketing Authorisations.
- SENIOR PHARMACOVIGILANCE SCIENTIST – Strategy, Safety, Submissions – Pharma Contract
Safety Surveillance, Contract – This globally established, Top 10 pharma are currently looking to secure a Senior Pharmacovigilance Scientists on a contract basis, 6 months. The roles will be ideally based in the North West, however home based flex can be considered beyond initial periods.
They require those with proven safety surveillance backgrounds, working at a high level in strategy, medical support so ideally PV Manager, Consultant or Director background
- Regulatory Affairs Manager CTA – West London
Regulatory Affairs Manager CTA - West London
My client, a dynamic company which is globally recognised as an extremely reputable company has an urgent opening for a Regulatory Affairs Manager CTA. The successful candidate will join the EU Regulatory Team based in the UK.