Source Job

$60,000–$70,000/yr
US

  • Manage end-to-end PV package preparation, quality control, and compliance tracking.
  • Oversee PV mailbox operations, query triage, and stakeholder communication.
  • Ensure inspection readiness through documentation governance and audit support.

Pharmacovigilance Document Management

4 jobs similar to Patient Safety Specialist

Jobs ranked by similarity.

US Unlimited PTO

  • Lead the strategy, planning, execution, and maintenance of safety databases and outsourced PV activities.
  • Oversee collection, evaluation, and reporting of safety data from clinical trials, shaping the safety governance framework.
  • Manage PV vendor contracts, quality/compliance for ICSR case processing, and mentor PV operations associates.

MapLight Therapeutics is a clinical stage biotech company focused on drug discovery for central nervous system disorders. It is a growing organization that values open dialogue and mutual respect while developing novel therapies for psychiatric symptoms.

$120,000–$250,000/yr
US

  • Provide medical oversight for clinical trials, safeguarding participant safety and ensuring protocol compliance.
  • Review adverse events and safety data, contributing to regulatory reporting and clinical documentation.
  • Collaborate with investigators and clinical teams to support study design, execution, and risk management.

This position is listed on behalf of a partner company that manages all applications and next steps. The role supports global clinical research in a remote working environment with cross-functional collaboration.

US Unlimited PTO

  • Drive global PV Operations strategy, including planning, implementation, and management, in alignment with the Head of DSPV.
  • Oversee vendor oversight, case management, compliance, inspection readiness, and budget/resourcing.
  • Represent DSPV Operations to senior leadership, manage talent, and ensure global regulatory compliance.

Vera Therapeutics is a commercial-stage biotechnology company focused on transforming medicine in autoimmune disease, starting with the kidney. Founded in 2016 and based in Brisbane, California, we foster a culture of empathy, owner's mindset, and urgency because patients are counting on us.

US

  • Provide strategic medical leadership for clinical safety across investigational therapies for pulmonary fibrosis.
  • Conduct hands-on medical review of serious adverse events and lead signal detection and benefit-risk assessments.
  • Oversee cross-functional safety review meetings and regulatory interactions.

The company is a clinical-stage biotechnology firm developing innovative therapies for pulmonary fibrosis and other serious respiratory diseases. It is a growing, lean organization with a focus on pharmacovigilance infrastructure and global clinical development.