Source Job

$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.

Pharmacovigilance Regulatory Compliance Clinical Trials

5 jobs similar to Pharmacovigilance Scientist

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.

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.

Oruka Therapeutics develops novel biologics for chronic skin diseases like plaque psoriasis. It is a growing biotechnology company with a startup culture focused on making a difference.

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.

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.

$150,000–$180,000/yr

  • Lead Medical Affairs workstreams including KTL engagement, congress activities, and scientific communications.
  • Develop and execute strategic medical plans, translating scientific evidence into actionable recommendations.
  • Provide scientific expertise across the product lifecycle, supporting clinical education and evidence communication.

Kaléo is a pharmaceutical company focused on developing life-saving auto-injector devices for patients. They are a lean, cross-functional organization with a passionate, purpose-driven culture and a highly collaborative, close-knit team.