- Senior Regulatory Affairs Manager (Associate Director Level) North Carolina - USA
An Excellent opportunity have arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company within the US - North Carolina - OFFICE based in the RTP - PERMANENT postion.
- Senior Manager/Associate Director - Regulatory Affairs-124726
PPD is seeking a Senior Manager/Associate Director to join their growing Global Regulatory Affairs (GRA) Department in the EMEA region.
In this role, you will provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization. ...
- Manager/Associate Director, Regulatory Affairs
NCR are working with a growing US Biotech to help source a Senior level Regulatory Affairs Professional. They have had great success with their proprietary technology, leading to promising treatments of Viral Infections. They are currently seeking an Associate Director, Regulatory Affairs to reside in their Central London, UK office.
- Regulatory Affairs Opportunities, Switzerland
Regulatory Affairs Opportunities for Pharmaceuticals, Switzerland, Zurich, Basel, Geneva and Bern
- Associate Director Regulatory Affairs - EMEA
Associate Director Regulatory Affairs - EMEA
Want to gain line-management experience in a large Bio-pharma? Are you looking to work for a company that has a specific development plan to progress your career
- Regulatory Affairs Manager, EU
Regulatory Affairs Manager, EU, Partner Collaboration in Europe for Established Products
- Regulatory Affairs Manager, Technical Focus
Regulatory Affairs Manager, Drug development, CMC, Basel area, Opportunity to work with complex molecules
- Drug Safety and Risk Management Associate (12 month contract)
Drug Safety and Risk Management Associate (12 month contract) - LondonMy client, an ever growing and cutting edge Biotech, is looking for someone to come in as a "Drug Safety and Risk Management Associate". This role will assist and support all of the drug safety and risk management activities for the affiliate. On offer is a 12month freelance contract.
- Senior Drug Safety Specialist – West London / Middlesex
Senior Drug Safety Specialist - West London / MiddlesexA great opportunity as been created for an experience Drug Safety Specialist. You will come into this global company to perform the case work and safety reporting for my client's clinical trials.
- Pharmacovigilance Associate
Drug Safety Associate - CambridgeshireAn exciting opportunity has become available for an experienced Drug Safety Associate to join this successful company. The placed candidate will join the dynamic and fast paced company and gain great exposure to the Drug Safety arena