Senior Pharmacovigilance Specialist

Placements24; Randburg; Presencial; ZAR 700 000 - 1 100 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive salary

Health insurance

Training opportunities

Paid leave

Retirement benefits

Resumo da oferta

Placements24 in Randburg is seeking a Senior Pharmacovigilance Specialist to join our client's safety surveillance team. You will lead adverse event data collection, assessment, and reporting, ensuring compliance with global requirements and robust risk management for post-market medicines.

The role requires 4–6 years in pharmacovigilance, a life sciences degree, strong analytical and communication skills, and the ability to manage multiple priorities in a dynamic environment.

Qualificações

• Bachelor's degree in Pharmacy, Nursing, Medicine, or a related healthcare field.
• Strong analytical, investigative and problem-solving abilities.
• Excellent written and verbal communication skills.

Responsabilidades

• Collect, process, and assess adverse event reports from various sources.
• Ensure timely and accurate reporting to regulatory authorities and stakeholders.
• Conduct literature reviews to identify potential safety signals and risks.
• Participate in development and implementation of risk management plans (RMPs).
• Maintain and update safety databases with data integrity and compliance.
• Contribute to preparation of PSURs/PBRERs.

Conhecimentos

Analytical skills

Investigative skills

Communication skills

Formação académica

Bachelor's degree in Pharmacy, Nursing, Medicine, or related healthcare/life science field

Ferramentas

Argus

ARISg

Descrição da oferta de emprego

About the Role

Our client is seeking a highly skilled and experienced Senior Pharmacovigilance Specialist to join their safety surveillance team in Randburg . This role is essential for ensuring the ongoing safety and monitoring of pharmaceutical products post-market. You will be responsible for collecting, assessing, and reporting adverse event data, maintaining compliance with global regulatory requirements, and contributing to risk management strategies. The ideal candidate possesses a deep understanding of pharmacovigilance principles, excellent analytical skills, and the ability to manage multiple priorities in a dynamic environment. Your contribution will be vital in protecting public health and ensuring the continued safe use of our client's medicines.

Key Responsibilities

• Collect, process, and assess adverse event reports from various sources.
• Ensure timely and accurate reporting of safety information to regulatory authorities and other stakeholders.
• Conduct literature reviews to identify potential safety signals and emerging risks.
• Participate in the development and implementation of risk management plans (RMPs).
• Maintain and update safety databases, ensuring data integrity and compliance.
• Contribute to the preparation of periodic safety update reports (PSURs/PBRERs).

Requirements

• Bachelor's degree in Pharmacy, Nursing, Medicine, or a related healthcare/life science field.
• Minimum of 4-6 years of experience in pharmacovigilance or drug safety.
• Thorough knowledge of pharmacovigilance regulations and guidelines (e.g., GVP, CIOMS, FDA, EMA).
• Experience with safety databases (e.g., Argus, ARISg) and adverse event reporting systems.
• Strong analytical, investigative, and problem-solving skills.
• Excellent written and verbal communication skills.

Benefits

• Competitive annual salary with potential for performance-based rewards.
• Comprehensive health, dental, and vision insurance.
• Opportunities for specialized training in pharmacovigilance and drug safety.
• Work within a well-established pharmaceutical company dedicated to patient safety.
• Generous annual leave and retirement benefits package.