An exciting small biotech company in the San Francisco Bay Area is in need of a strong GCP Quality Assurance Consultant. With 2 studies well within their respective phase I and II clinical trials - the team is looking to expand!
Considering the team sits within a start-up environment and has an influx of series B funding - they are prepared to make their company a household name!
The clinical quality team is seeking strong experience within phase I-II experience in the therapeutic areas of Cardiovascular and Pulmonary diseases. The role requires 10+ years industry experience, SOP writing/revisions, inspection readiness, QMS, risk management, clinical study reports, audit, and vendor management experience.
If you'd like to learn more about the role, get a full JD, name of the company, remote/on-site expectations etc. please feel free to reach out/apply/send a CV.
