Pharmacovigilance Specialist

Placements24; Klerksdorp; Hybrid; ZAR 450,000 - 650,000; Full time

Benefits offered by this job

Remote work

Health insurance

Job summary

Placements24 is seeking a diligent Pharmacovigilance Specialist for a fully remote role in South Africa. You will monitor safety profiles of pharmaceutical products, collect and evaluate adverse events, and ensure compliance with SAHPRA and international guidelines.

The ideal candidate holds a Pharmacy/Medicine/Nursing degree and has at least 3 years of pharmacovigilance experience, with strong data analysis and clear written and verbal communication skills for cross‑functional collaboration.

Qualifications

• Degree in Pharmacy/Medicine/Nursing or life science.
• Minimum of 3 years in pharmacovigilance or drug safety.
• Knowledge of SAHPRA, FDA, EMA and related regulations.

Responsibilities

• Collect, process, and evaluate adverse event reports from various sources.
• Conduct medical reviews of adverse event data for regulatory reporting.
• Prepare and submit PSURs and other regulatory safety documents.
• Maintain pharmacovigilance database ensuring data integrity.
• Develop and update SOPs related to pharmacovigilance activities.
• Collaborate with internal/external stakeholders to manage safety information.

Skills

Pharmacovigilance

Adverse event reporting

Regulatory knowledge

Data analysis

Education

Pharmacy/Medicine/Nursing degree

Tools

Safety databases

Job description

Our client is seeking a diligent and experienced Pharmacovigilance Specialist for a fully remote position, allowing you to contribute to patient safety from anywhere in South Africa . This role is essential for monitoring the safety profiles of our client's pharmaceutical products and ensuring compliance with global and local pharmacovigilance regulations. You will be responsible for the collection, assessment, and reporting of adverse event data, playing a critical role in safeguarding public health. This is an excellent opportunity for a meticulous professional to make a significant impact in a vital area of pharmaceutical safety, working within a globally recognized organization that values scientific integrity and employee well-being.

Key Responsibilities

• Collect, process, and evaluate adverse event reports from various sources, ensuring accuracy and completeness.


• Conduct medical reviews of adverse event data and determine appropriate regulatory reporting.


• Prepare and submit periodic safety update reports (PSURs) and other regulatory safety documents.


• Maintain and manage the pharmacovigilance database, ensuring data integrity and compliance.


• Develop and update Standard Operating Procedures (SOPs) related to pharmacovigilance activities.


• Collaborate with internal departments (e.g., Medical, Regulatory, Clinical) and external stakeholders to manage safety information.

Requirements

• Degree in Pharmacy, Medicine, Nursing, or other relevant life science discipline.


• Minimum of 3 years of experience in pharmacovigilance or drug safety.


• Thorough understanding of global and local pharmacovigilance regulations (e.g., SAHPRA, FDA, EMA).


• Experience with safety databases and adverse event reporting systems.


• Strong analytical skills and meticulous attention to detail.


• Excellent written and verbal communication skills, with the ability to work independently in a remote environment .

Benefits

• Competitive salary and remote work benefits.


• Comprehensive health, dental, and vision insurance.


• Generous annual leave and paid time off.


• Opportunities for professional development and continuous learning in drug safety.


• A supportive and collaborative virtual team culture focused on patient safety.