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• Boston
• US$115.50 - US$160 per hour
• Posted about 9 hours ago

Fully-Remote: Reg. Affairs Consultant Clinical stage biotech that aims to lead the development of experimental allogeneic chimeric antigen receptor T cell treatments for cancer. Our team of researchers is committed to discovery and translational research, development and cell manufacturing and is...

• Delaware
• Negotiable
• Posted 3 days ago

- Author and manage ALL clinical documents while establishing timelines for clinical study protocols, clinical study reports, investigator's brochures, clinical technical components, risk management plans and module summaries - Author IND/CTA and global regulatory submission documents - Actively ...

• Palo Alto
• US$75 - US$95 per hour
• Posted 4 days ago

Manager, Regulatory Affairs A specialty pharmaceutical company is currently seeking a Manager Regulatory Affairs to join their team to assist in supporting and developing regulatory strategies. This position is an onsite Contract to Hire role in Palo Alto, CA and reports to the Senior Director Re...

• United States of America
• Negotiable
• Posted 7 days ago

Director/Senior Director Regulatory Affairs A Clinical Stage biotechnology company that is focusing in tumor targeted therapies is currently seeking a Director/Senior Director regulatory affairs to join the team for a remote contract. Responsibilities: Assist in development and implementation of ...

• Seoul
• Negotiable
• Posted 10 days ago

My client is a global medical device company, headquartered in the US, specialising in Orthopaedics and General Surgery medical devices. They are looking for a RAQA expert for their Korea Team. Responsibilities: Registration of new products Review and attaining of KGMP certificates KGMP Submissio...