Our client, an oncology-focused biotech company in Cambridge, is looking to fill a high-level safety/pharmacovigilance need. This is a long-term contract role. Duties include: Contributing to safety sections of key clinical/regulatory documents, developing the PV long-term plan and infrastructure, providing clinical assessment of SAE cases, signal detection, and more. Candidate should either have an MD or PharmD with at least 5 years of experience in the biopharma industry, doing safety work.
Please reply with a copy of your CV if this role is a fit. Many thanks!