Clinical Development Jobs
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Senior Regulatory Affairs Specialist
Job Description:This role will be primarily focused on registrations outside of the US. The responsibilities include:Prepare and submit global regulatory applications, (Pre-Submissions, 510ks, IDEs and applicable supplements and annual reports) in countries such as Japan, India, China, Saudi Arabia, Australia, Mexico and Brazil.Support U.S. Medical...
Executive Medical Director Pulmonology
Executive Medical Director Clinical Development Greater Boston Area - Hybrid Compensation: $250,000-290,000 + 25% bonus + Lucrative RSU package Company Summary: We have partnered with a mid-sized biotech company at the forefront of developing innovative therapeutic products for endocrine and orphan lung diseases. They already have two key produc...
Senior Manager Regulatory Affairs
Title: Senior Manager Regulatory AffairsA leading global Medical Device company is seeking a Senior Manager of Regulatory Affairs to join their team on-site in their downtown Atlanta office. This new team member will be responsible for the management and leadership of the Regulatory Affairs department, allocating and managing department resources t...
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Manager, TMF Operations
Exciting Opportunity: Manager, TMF OperationsWe're partnering with an innovative clinical-stage biopharmaceutical company to find a skilled Manager, Trial Master File (TMF) Operations. This is a fantastic opportunity to join a fast-paced environment at the forefront of transformative drug development. In this highly visible role, you'll play a key ...
Director Clinical Scientist
Director Clinical Scientist Salary: $230,000 - $275,000 New York City (On Site) Job DescriptionEPM is partnered with a clinical-stage biotech company that is creating innovative therapeis to treat patients with unmet medical needs in the Autoimmune, Fibrotic, and CNS space. With multi million dollar partnerships with peers in the industry, this opp...
SR Manager/AD Medical Writing
Key ResponsibilitiesLead or contribute to the preparation of clinical documents, including but not limited to protocols, CSRs, DSURs, IBs, safety narratives, and related appendices.Collaborate cross-functionally with Clinical Operations, Regulatory, Safety, and Biostatistics to ensure alignment and accuracy across all deliverables.Manage multiple w...