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© All Rights Reserved. ApplyBlast.com
Octapharma
The role supports the Clinical Research and Development team by setting up and maintaining Trial Master Files and Investigator Site Files, preparing clinical trial documentation for regulatory submissions, and ensuring audit and inspection readiness. The position also acts as a central contact for trial documentation, assists with investigator meetings, and performs various administrative tasks to aid clinical trial execution.
Octapharma is a global biopharmaceutical company that develops and manufactures plasma-derived and recombinant therapies for patients worldwide. The company specializes in haematology, immunotherapy, and critical care, producing medicines based on proteins derived from human cell lines and human plasma. Octapharma is one of the largest human protein manufacturers in the world, operating multiple state-of-the-art manufacturing sites globally.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Octapharma.
Octapharma didn’t post a salary, so this is our estimate from similar listings.
30% below the average for this role