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Found 83 jobs
Minimum 12 month contract for a medical information / scientific advisor / MSL professional within medical affairs with a global pharma client
GDP Quality professional required to join our client in a minimum 12 month contract based in Berkshire
We have an exciting opportunity for a medical writer/senior medical writer who loves to develop publications based on HEOR data.
Fast paced, cutting edge T-Cell Biotechnology company looking to expand their CMC team.
Global Regulatory Operations Publishing Manager - Biopharma Flexible working arrangements - a combination of WFH and On-site. Excellent opportunit
The role will work closely with the Director of Quality and staff to advise and oversee GCP compliance in the Clinical and Medical group.
Full-time permanent opportunity for a post-marketing PV professional looking to move into a medical affairs role
Job Summary We are looking for a Senior/Principal Scientist to join our Cellular Immunology group who has a deep passion for immunology and the rol...
Minimum 12 months FTC for a med info/medical affairs professional with copy approval experience looking to take on an international copy approval role
If you are looking for career progression, personal growth, and development, this is the opportunity for you!
Senior Bioinformatician I am working with a Biotechnology company in Oxford who is recruiting for a Senior Bioinformatician to join their team. The
Cpl Life Sciences have partnered once again with an innovative and growing business looking to bring on board an Associate Medical Director Officer.
Albion Rye Associates are delighted to be supporting one of our longest standing Medical Communications clients on a multi-hire project within thei...
We are looking for a Scientist to join our Cellular Immunology group who has a deep passion for immunology and the role of T-cells in the exciting ...
PsiOxus Therapeutics Ltd is an award-winning UK/US development stage biotechnology company developing novel therapeutics for the treatment of cance...
PsiOxus Therapeutics Ltd is an award-winning UK/US development stage biotechnology company developing novel therapeutics for the treatment of...
Manager, UK Regulatory Affairs!! Project Manage and Lead UK Submissions - Biologics and Pharma Products, but no prior Biotech product experience is re
Senior Director, Regulatory Affairs - ATMP/Gene Therapies. Global Regulatory Lead - EU and International. Primary point of contact with the Regulatory
Our employees are able to develop their careers in exciting new medical technologies, and so can you.
Our employees are able to develop their careers in exciting new medical technologies, and so can you. Oxford Biomedica’s Process R&D team consists of