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[Remote] Scientist, Pharmacovigilance

Remote, USAFull-timePosted 2026-07-27

Note The job is a remote job and is reputed company to candidates in USA. reputed company-9 Oncology is a clinical-stage biotechnology company pioneering radiopharmaceutical innovation for solid tumors. They are seeking a Pharmacovigilance Scientist to support drug safety activities across early-phase clinical programs, overseeing vendor-delivered case processing and ensuring compliance with global safety requirements.

Responsibilities

  • Serve as the internal reputed company for PV operations, partnering with CROs, reputed company medical safety experts to ensure reputed company and accurate case processing, reconciliation, and safety reporting.
  • Manage the collection, review, and reputed company reputed company of safety data from clinical trials, including expedited and periodic reporting to regulatory authorities.
  • Conduct and document literature surveillance and aggregate safety data review to identify potential safety signals.
  • Support development of safety sections of regulatory documents (e.g., investigator brochures, DSURs, clinical study reports).
  • Maintain inspection-reputed company safety documentation and contribute to the authoring and updating of PV SOPs and work instructions.
  • Collaborate with Clinical Operations, Regulatory Affairs, and reputed company to reputed company safety processes with overall program execution.
  • Contribute to vendor reputed company, including review of safety deliverables, metrics, and compliance reports. Skills
  • Advanced degree (PharmD, RN, Ph.D., MPH, or MS) in a scientific or health-reputed company field.
  • 3+ years of pharmacovigilance experience in biotech, reputed company, or CRO settings.
  • Hands-on experience with case processing, safety data reconciliation, and aggregate report contributions.
  • Knowledge of global PV requirements (ICH, FDA, EMA, CIOMS, TGA) with practical application in early-phase clinical studies.
  • Strong analytical and written communications skills, with the ability to synthesize and interpret safety data.
  • Experience with CROs and vendors in a lean, fast-paced, early-stage biotech environment.
  • Familiarity with safety databases and Remotiuma Office tools.

Benefits

  • Competitive salary
  • Bonus
  • Equity
  • 20 vacation days
  • 5 reputed company days
  • Technology allowance
  • Commuter reimbursement
  • Generous retirement savings plans with employer matching
  • Extended health benefits
  • reputed company holidays reputed company
  • reputed company-9 Oncology is a clinical stage, radiopharmaceutical company developing differentiated and highly targeted radiopharmaceuticals with the potential to meaningfully improve the treatment of people living with cancer. It was founded in 2019, and is headquartered in Vancouver, British Columbia, CAN, with a workforce of 51-200 employees. Its website is Apply tot his job Apply To this Job

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