FDA Submissions & Documentation Specialist

A biopharmaceutical company in San Francisco is seeking someone to support the creation and coordination of operational deliverables for FDA submissions. The ideal candidate will have a bachelor’s degree in Life Science or Business Administration, alongside 3-4 years of experience in the pharmaceutical or biotech sectors, particularly in clinical trial documentation management. Responsibilities include performing quality checks on submissions and ensuring compliance with regulatory guidelines. This role is crucial in supporting Clinical Trials. #J-18808-Ljbffr