Regulatory jobs

• United States of America
• US$65000 - US$80000 per annum
• Posted 1 day ago

Our client is on the lookout for a proficient Content Developer to produce engaging, customer-centric instructional materials. In this role, you will be responsible for creating and maintaining a wide array of user-friendly Instructions for Use (IFU) documents, such as Operator's Manuals, Quick R...

• Northern Ireland
• Negotiable
• Posted 22 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clinical trials. GAP Asse...

• Northern Ireland
• Negotiable
• Posted 22 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clini...

• Irvine
• Negotiable
• Posted 22 days ago

Title: Regulatory Affairs Senior Manager Summary: Our client is seeking an experienced Senior Manager of Regulatory Affairs to lead the preparation and submission of global regulatory filings, ensuring compliance with clinical, pre-, and post-market requirements. This role involves cross-function...

• Northern Ireland
• Negotiable
• Posted 29 days ago

We have a current opportunity for a Senior Clinical Project Manager working with IVDs on a contract basis. 6 months contract (possible extension) Clinical protocols, risk management plans, knowledge of IVD regulation within Europe Client-facing position (face-to-face) Remote with occasional site ...

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

• New York
• Negotiable
• Posted about 2 months 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...