Contract Regulatory Jobs
Showing 7 results
Sort by:
CMC Submission Lead
CMC Submission Lead | 12-Month Contract | Fully Remote (Europe)We are supporting a global pharmaceutical and biotechnology organisation seeking an experienced CMC Submission Lead to support high-profile regulatory submissions across both development-stage and commercial products.This role will be responsible for leading and coordinating CMC submiss...
CMC Submission Lead
CMC Submission Lead12-Month Contract | Remote (Europe)Pharmaceutical / Biotechnology SectorOverviewWe are supporting a global pharmaceutical and biotechnology organisation seeking an experienced CMC Submission Lead to support a portfolio of regulatory submission activities across development and commercial products.This contract opportunity will pl...
Regulatory Affairs CMC Speciaist
Regulatory CMC ConsultantContract: 18 Months Location: Copenhagen, Denmark (Fully Remote) Industry: Vaccines / Global Public HealthWe are supporting a leading pharmaceutical organisation on a high-profile Tuberculosis (TB) vaccine development programme and are looking for an experienced Regulatory CMC Consultant to join the team on an 18-month cont...
Elevate your career
Take the first step toward your next opportunity - submit your resume and get started today.
Global Regulatory affairs specialist
Principal Regulatory Affairs Opportunity - Global Semaglutide PortfolioWe are supporting a leading global pharmaceutical company in the search for a Principal Regulatory Affairs professional to join a high-profile regulatory team responsible for post-marketing activities across a market-leading chronic disease portfolio.This position offers the opp...
Regulatory Affairs Specialist
I'm currently looking for a CMC Regulatory Affairs Specialist with strong experience in late-stage development, EU regulatory submissions, and vaccines/biologics products, with a particular focus on tuberculosis (TB) vaccines. Candidates with broader public health vaccine experience in biologics environments will also be considered, but vaccine exp...
Reg affairs
I'm currently looking for a CMC Regulatory Affairs Specialist with strong experience in late-stage development, EU regulatory submissions, and vaccines/biologics products, with a particular focus on tuberculosis (TB) vaccines. Candidates with broader public health vaccine experience in biologics environments will also be considered, but vaccine exp...