Regulatory jobs

• United States of America
• Negotiable
• Posted 2 days ago

* Authoring high-quality CMC documentation for US/ EU / UK countries, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. * P...

• Nottingham
• Negotiable
• Posted 2 days ago

We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.

• United States of America
• Negotiable
• Posted 4 days ago

A leading organization in the pharmaceutical and regulatory affairs industry, dedicated to increasing project efficiency and establishing project management standards; are looking for a talented and experienced Project Manager to join the Project Management Office (PMO) team. Key Responsibilities...

• New Jersey
• Negotiable
• Posted 8 days ago

Title: Regulatory Affairs Senior Manager Summary: A leading, global pharmaceutical client of ours is looking to hire a Senior Manager of Regulatory Affairs at their prescription drug specific subsidiary, based out of New Jersey. This rapidly growing client has drugs spanning many different therap...

• Massachusetts
• US$175000 - US$195000 per annum
• Posted 10 days ago

Title: Associate Director Regulatory Affairs A small but growing clinical stage company is seeking an Associate Director Regulatory Affairs to join the team in a remote capacity. They are seeking a well-rounded RA professional to lead the Regulatory Strategy for their pipeline of phase III produc...

• New York
• Negotiable
• Posted 18 days ago

Regulatory Affairs Manager - Pharma (Remote - East Coast Preferred) A global leader in drug delivery systems is seeking a Regulatory Affairs Manager to support U.S. regulatory activities across multiple business divisions. This role will be instrumental in defining regulatory strategies, ensuring...

• Boston
• US$160000 - US$190000 per annum
• Posted 22 days ago

Title: Associate Director Regulatory Affairs A small but growing clinical stage company is seeking an Associate Director Regulatory Affairs to join the team in a remote capacity. They are seeking a well-rounded RA professional to lead the Regulatory Strategy for their pipeline of phase III produc...

• Negotiable
• Posted about 1 month ago

Role: Leasing Manager Location: Ireland (Homebased) About the Company: A global market leader in the Life Sciences testing space is searching for a Head of Asset Management to join the team. Responsibilities: Asset management - You will be fully responsible for the inventory, deployment and lifec...

• Japan
• Negotiable
• Posted about 1 month ago

Job Title: Regulatory Affairs Director Location: Japan (Remote) Our client is a global pharmaceutical company dedicated to improving global health through innovative pharmaceutical solutions. Their commitment to excellence and patient care drives them to develop and deliver high-quality medicatio...

• Boston
• US$160000 - US$190000 per annum
• Posted about 1 month ago

Title: Associate Director Regulatory Affairs A small but growing clinical stage company is seeking an Associate Director Regulatory Affairs to join the team in a remote capacity. They are seeking a well-rounded RA professional to lead the Regulatory Strategy for their pipeline of phase III produc...

• United States of America
• Negotiable
• Posted about 1 month ago

Regulatory Affairs Contractor (Remote, USA) As a Regulatory Affairs Contractor, you will support the development and implementation of global regulatory CMC strategies for our partners' marketed and development products. You will assist with regulatory activities for both internal and external pr...

• United States of America
• Negotiable
• Posted about 1 month ago

Job Overview The Clinical Evaluation Reporting Specialist is tasked with creating Clinical Evaluation Reports (CERs) for Terumo Blood and Cell Technologies (TBCT) products. This involves utilizing product labeling, preclinical and clinical data, published literature, risk management documents, co...