Remote Pharmacovigilance Specialist – Drug Safety & Growth

Placements24

South Africa

Remote

ZAR 520,000 - 860,000

Full time

4 days ago
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Benefits offered by this job

Remote work benefits package

Job summary

Placements24, in partnership with a global biopharmaceutical leader, seeks a Remote Pharmacovigilance Specialist to monitor, assess, and report adverse events. This fully remote role enables you to contribute to drug safety from anywhere in South Africa, collaborating with a distributed global team.

The ideal candidate has a Bachelor's in a healthcare field and at least 3 years in pharmacovigilance, with strong knowledge of ICH-GCP, GVP, and MedDRA.

Qualifications

  • Minimum 3 years of experience in pharmacovigilance or drug safety.
  • Experience with adverse event case processing and regulatory reporting.
  • Strong knowledge of ICH-GCP, GVP guidelines, and regulatory requirements.

Responsibilities

  • Collect, process, and evaluate adverse event reports from various sources.
  • Enter data accurately into safety databases.
  • Code adverse events using MedDRA or WHO-DD terms.
  • Prepare and submit regulatory safety reports within defined timelines.
  • Collaborate with internal and external partners to gather case information.
  • Support development and maintenance of pharmacovigilance procedures and guidelines.
  • Participate in safety surveillance activities and risk management planning.
  • Stay updated on global pharmacovigilance regulations.

Skills

Pharmacovigilance
Regulatory reporting
Adverse event processing
ICH-GCP
GVP guidelines
Safety databases
MedDRA/WHO-DD
Remote teamwork

Education

Bachelor's degree in Pharmacy, Nursing, Life Sciences

Tools

Safety databases
Data entry systems
MedDRA/WHO-DD dictionaries

Job description

Placements24, in partnership with a global biopharmaceutical leader, seeks a Remote Pharmacovigilance Specialist to monitor, assess, and report adverse events. This fully remote role enables you to contribute to drug safety from anywhere in South Africa, collaborating with a distributed global team.

The ideal candidate has a Bachelor's in a healthcare field and at least 3 years in pharmacovigilance, with strong knowledge of ICH-GCP, GVP, and MedDRA.

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