Remote Drug Safety Physician | Lead Pharmacovigilance

Placements24

Midrand

Hybrid

ZAR 1,200,000 - 1,800,000

Full time

5 days ago
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Benefits offered by this job

Fully remote work
Competitive salary
Globally focused role
Professional development opportunities

Job summary

Placements24 is seeking a highly qualified Remote Drug Safety Physician to strengthen its pharmacovigilance team. The physician will assess adverse event data, lead signal detection, and contribute to global regulatory safety reporting from a home office.

Ideal candidates have 5–7 years in pharmacovigilance, MD or equivalent training, and board certification in a relevant specialty. The role emphasizes independent work and collaboration with regulators worldwide.

Qualifications

  • MD or equivalent medical degree.
  • 5–7 years of pharmacovigilance/drug safety experience.
  • Experience in PSUR/DSUR preparation and regulatory safety documents.
  • In-depth knowledge of global pharmacovigilance regulations and reporting.

Responsibilities

  • Perform medical review of adverse event reports.
  • Lead signal detection and safety evaluation activities.
  • Contribute to PSURs, DSURs and regulatory safety documents.
  • Provide medical guidance to regulatory, clinical and R&D teams.
  • Collaborate on risk management plans (RMPs).
  • Serve as medical contact for regulatory agencies.
  • Support safety risk-benefit assessments and lifecycle decisions.
  • Ensure compliance with global pharmacovigilance guidelines.
  • Mentor remote drug safety team members.

Skills

Pharmacovigilance
Clinical medicine
Signal detection
Risk assessment
Analytical thinking
Communication skills
Remote collaboration

Education

MD or equivalent
Board certification in a relevant specialty

Job description

Placements24 is seeking a highly qualified Remote Drug Safety Physician to strengthen its pharmacovigilance team. The physician will assess adverse event data, lead signal detection, and contribute to global regulatory safety reporting from a home office.

Ideal candidates have 5–7 years in pharmacovigilance, MD or equivalent training, and board certification in a relevant specialty. The role emphasizes independent work and collaboration with regulators worldwide.

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