Pharmacovigilance Study Officer – 10 Openings

About the role

The Consultant Pharmacovigilance Study Officers will support the design, implementation and monitoring of pharmacovigilance studies focused on medicine and vaccine safety. This full‑time, on‑site position in Turkwel involves daily collection, verification and analysis of safety data to protect public health.

Key responsibilities

• Collect, verify and enter safety data into pharmacovigilance databases.
• Conduct case follow‑ups and ensure protocol and ethical compliance.
• Develop study tools and train facility staff on adverse event reporting.
• Assist with data management, analysis and interpretation of safety signals.
• Prepare summary reports, study documentation and technical summaries.
• Collaborate with clinical teams, local health authorities and project managers.
• Participate in coordination meetings, quality‑assurance activities and continuous improvement of pharmacovigilance processes.

Required profile

• Background in pharmacy, medicine, nursing, public health or a related health discipline.
• Strong knowledge of pharmacology and drug‑safety principles.
• Experience in pharmacovigilance, clinical research or epidemiological studies.
• Excellent written and verbal communication skills.
• Ability to work on‑site in Turkwel and engage respectfully with communities and authorities.
• Attention to detail, critical thinking and problem‑solving abilities.
• Familiarity with ethical principles in human‑subject research; regulatory experience is a plus.
• Proficiency in basic computer applications and willingness to learn new digital systems.

Required skills

• Data management and analysis using spreadsheets and statistical tools.
• Accurate record‑keeping and preparation of technical summaries.
• Use of MS Office applications.
• Experience with pharmacovigilance databases and digital data‑collection systems.