- 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. ...
- CMC Regulatory Affairs Associate Director, New Challenge!
Global Regulatory CMC Associate Director, Small Molecules, New Department, Early Development, Strategic and Hands on Input, 160-200k CHF
- 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.
- Drug Safety and Risk Management Associate - London
Drug Safety and Risk Management Associate - 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.
- 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