Source Job

US

  • Lead product safety surveillance strategies and risk management for investigational products.
  • Oversee medical review of safety data and ensure compliance with global pharmacovigilance regulations.
  • Build pharmacovigilance infrastructure and manage vendor partnerships as the company grows.

Pharmacovigilance Regulatory Compliance

5 jobs similar to Senior Medical Director, Pharmacovigilance and Safety

Jobs ranked by similarity.

$200,000–$245,000/yr
US

  • Lead risk management and safety data review for assigned products, ensuring regulatory compliance.
  • Provide safety-related content for clinical and regulatory documents, and prepare for inspections.
  • Mentor a small pharmacovigilance team while driving end-to-end operational oversight.

Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies for blood cancer patients. We maintain a start-up culture of camaraderie and leadership by example, with a small dedicated team.

Global

  • Lead safety evaluations and benefit-risk assessments for assigned products.
  • Provide medical leadership for pharmacovigilance activities across development and marketed products.
  • Support regulatory submissions and health authority interactions, including preparing responses to RFIs.

Alphanumeric is a staffing and recruiting company that places professionals in contract roles with top organizations. This role is a 1-year contract with a major pharmaceutical company, supporting its global Safety Evaluation & Risk Management function.

$130,000–$161,000/yr
US

  • Collects, reviews, and analyzes adverse event reports from clinical trials to identify potential safety signals.
  • Supports the preparation and review of pharmacovigilance documents such as DSURs, dRMPs, and relevant clinical trial sections.
  • Collaborates with cross-functional teams including clinical operations, regulatory affairs, and medical affairs.

Oruka Therapeutics is developing novel biologics designed to set a new standard for treating chronic skin diseases like plaque psoriasis. They are an early-stage public company (Nasdaq: ORKA) building a core team, seeking top talent to contribute to an engaged, inclusive, and positive culture.

India

  • Help implement and maintain new features within the Veeva Safety suite.
  • Work closely with customer business and IT staff to understand and design solutions.
  • Guide customers in adopting Vault and industry best practices for post-implementation success.

Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies accelerate therapies to patients. As a fast-growing SaaS company surpassing $3B in revenue, it operates as a public benefit corporation balancing customer, employee, society, and investor interests.

$108,000–$172,800/yr
Europe

  • Advise product and engineering teams on end-to-end safety case workflows including intake, triage, validation, and data reconciliation.
  • Review and verify AI-driven platform outputs to ensure precision, accuracy, and safety compliance across case processing.
  • Translate macro industry trends and operational shifts in PV into actionable platform capabilities and long-term automation strategies.

Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue last fiscal year and are legally bound as a public benefit corporation to balance the interests of customers, employees, society, and investors.