Pharmacovigilance Officer

Protect patients, ensure compliance—join us as a Pharmacovigilance  Officer and make safety your mission.

R&D Partners is working alongside a pharmaceutical company. We are seeking a Pharmacovigilance Officer to manage global safety data and support Medical Affairs activities. You will work closely with QPPV, internal teams, and external partners to ensure compliance with pharmacovigilance regulations and maintain patient safety.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• Manage safety data from receipt to regulatory reporting and audits.
• Process ICSRs, literature review, and maintain PV agreements.
• Support signal detection, aggregate safety reports (PSURs, PBRERs), and benefit–risk assessments.
• Contribute to Risk Management Plans and additional risk minimisation measures.
• Assist with product labelling, regulatory submissions, and horizon scanning.

Requirements:

• Degree in Biological or Biomedical Sciences (postgraduate preferred).
• Experience in pharmacovigilance, including case processing and data entry.
• Knowledge of PV legislation and Oracle Argus Safety Database (advantageous).
• Strong communication and medical writing skills.
• Ability to manage multiple priorities and work cross-functionally.

For more information, please contact William Tyler.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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