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Associate Director, Clinical Operations
EPM Scientific are partnered with a fast-growing, clinical-stage biotech who are redefining treatment paradigms with cutting-edge bispecific antibody therapies for immune and inflammatory disorders. Backed by strong investors and powered by a lean, agile team, this company is on a mission to deliver transformative biologics for patients with comple...
Freelance Medical Copyeditor
Freelance Medical Copy-EditorEPM is proud to be partnered with a globally recognised medical communications agency that is seeking additional support early next year. Our partner is known for delivering high-quality, scientifically accurate content across a wide range of therapy areas. With a vibrant and experienced team, they have recently experie...
Clinical Scientist 6 Month Contract
EPM Scientific are currently partnered with Biotech with an exciting & diverse pipeline. They are urgently seeking a Clinical Scientist to support their expanding clinical development team. See a short summary below:Role Overview:Ideal Start Date: December, FlexibleLocation: New Jersey, RemoteContract Type: 6-Month Contract, Full TimeLanguage: Engl...
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Senior Director/Vice President Regulatory Affairs Policy
A leading global biosimilars organization is seeking a Senior Director or Vice President, Regulatory Affairs to join its U.S. leadership team. This individual will serve as a key regulatory spokesperson and thought leader, supporting regulatory strategy for biosimilar products, shaping external policy engagement, and leading strategic interactions ...
Senior Director Business Development
Senior Director of Business Development - HCP EngagementDeveloping and executing sales strategies targeting pharmaceutical and biotech companies.Leveraging HCP engagement expertise to position educational solutions effectively.Hunt for and manage high-value accounts while negotiating complex contracts. Location: NY/MA (Remote)Salary: $175,000-$200,...
SR Manager/Associate Director Med Writing
Regulatory Writing & Document DevelopmentLead the creation of key regulatory documents, including clinical overviews, summaries, and study-specific content for major submissions.Draft and update clinical study reports, investigator brochures, and standard operating procedures.Contribute to protocols, amendments, statistical analysis outputs, briefi...