Lead adverse event assessment and regulatory reporting as a Remote Pharmacovigilance Specialist supporting drug safety operations across South Africa. Work fully remotely with global teams.
This experienced specialist supports safety surveillance for marketed and investigational pharmaceutical products. Responsibilities include adverse event processing, safety database use, signal detection, and risk management. The work requires regulatory knowledge and careful communication with internal teams and external stakeholders.
Key Responsibilities:
- Collect, process, and assess adverse event reports from varied sources
- Report safety cases accurately to authorities and stakeholders
- Maintain safety databases and adverse event information
- Prepare PSURs, PBRERs, and additional safety documents
- Support signal detection and risk management activities
Requirements:
- Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related healthcare field
- Minimum three years of pharmacovigilance or drug safety experience
- Knowledge of FDA, EMA, and ICH pharmacovigilance guidelines
- Experience with Argus, ArisG, or similar safety databases
- Strong medical terminology, analytical, and case processing skills
Apply pharmacovigilance expertise, regulatory reporting knowledge, and safety database experience to protect patients through remote work.
Remote Pharmacovigilance Specialist South Africa in Kimberley employer: Placements24
Join a forward-thinking company that values innovation and offers a fully remote work environment, allowing you to thrive from anywhere in South Africa. With a highly competitive salary, significant bonus potential, and a generous budget for professional development, this role as Legal Counsel - Intellectual Property not only provides the opportunity to protect and manage a diverse IP portfolio but also fosters a culture of growth and collaboration. Embrace the chance to work on cutting-edge technology while shaping the future of the company's intellectual property.
