Pharmacovigilance Scientist

Senior PV Scientist (Pharmacovigilance Scientist) We’re seeking a Senior PV Scientist to support safety and risk management activities for investigational and marketed products within an oncology portfolio. This role partners closely with the Safety Physician to evaluate, interpret, and communicate product safety data while ensuring compliance with global regulations.

Key Responsibilities

Lead safety analytics and signal management for assigned products

Author and coordinate aggregate safety reports (DSURs, PSURs, PADERs)

Review and contribute to clinical and regulatory documents (protocols, IBs, CRFs, ICFs)

Manage safety queries, data analyses, and health hazard evaluations

Collaborate cross-functionally with Safety, Biostatistics, Clinical, and Regulatory teams

Support process improvement initiatives and ensure compliance with PV standards

Qualifications

Advanced degree

(PharmD, RN, MD, PhD, MPH, NP, or equivalent)

5+ years of relevant medical, scientific, or pharmaceutical experience, including 3+ years in pharmacovigilance or drug safety

Must have experience in mental health or neurology

Strong analytical, communication, and project management skills

Proficiency in Excel, PowerPoint, and safety database systems (e.g., Argus)

Employment type Contract (6-month)

Senior level Mid-Senior level

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