Job opening
Sr. Pharmacovigilance (PV) Clinical Scientist
Filed under Pharmaceutical Manufacturing
Full job description
Job Title: Sr. Pharmacovigilance (PV) Clinical Scientist
Location: South San Francisco, CA 94080
Duration: 6 months contract (with possible extension)
Terms: Contract W2
Working Model: Hybrid
Working Days: Monday through Friday
Working Hours: 8 AM to 4:30 PM PT
Interview Format: Two Rounds (1. Hiring Manager [30 minutes]; 2. Upper Management [30 minutes])
Summary of Position
- The US Patient Safety Sr. PV Clinical Scientist - Pharmacovigilance (PV) Compliance Team performs the tactical and operational job responsibilities, including but not limited to the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Patient Safety.
- The Sr. PV Clinical Scientist leads clinical review of USPS cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director-PV Compliance Team in all activities.
- All responsibilities are performed under the direction of the US Patient Safety PV Clinical Management. Contributes in depth knowledge of Individual Case Safety Reports (ICSRs) case processing.
- Has developed a variety of skills typically gained through years of professional experience. Works autonomously with minimal supervision.
- May lead or contribute with skills to projects.
- May act as coach for colleagues with less experience and provide guidance.