Introduction
Our client is a long-established organisation in the specialist pharmaceuticals sector, supplying essential injectable medicines used across critical care settings. They operate within an international group with a strong reputation for product quality, patient safety and collaborative working. The team you would be joining is known for its supportive environment, cross-functional cooperation and commitment to continuous improvement, offering an excellent culture for individuals who enjoy both structure and autonomy.
This role will offer you
* The chance to work in a globally connected Medical Affairs function with exposure to international partners and regulatory authorities.
* A meaningful role where your work directly supports patient safety and compliance across a broad portfolio of critical medicines.
* Professional growth through involvement in advanced PV activities such as signal management, aggregate reporting and risk management.
* An opportunity to influence best practice through process improvement, SOP development and collaboration with senior leaders including the QPPV.
You will be responsible for
* Managing the end-to-end handling of global safety data, from initial receipt through to assessment and regulatory reporting.
* Maintaining strong working relationships with worldwide business partners to ensure the compliant exchange of safety information.
* Contributing to literature reviews, SOP development and PV agreement oversight as part of the wider quality and compliance framework.
* Supporting activities such as signal detection, aggregate safety reporting, benefit–risk assessments and risk management planning.
* Assisting with Medical Affairs outputs including product labelling, regulatory submissions and lifecycle maintenance.
You will bring the following
* A degree in Biological or Biomedical Sciences (postgraduate study advantageous).
* Proven experience in pharmacovigilance, ideally including case processing and use of safety databases such as Oracle Argus.
* Strong understanding of PV legislation, data handling principles and regulatory expectations.
The Ending
If you’re interested in joining a supportive, growing Medical Affairs/Pharmacovigilance team and would like to learn more about this opportunity, please get in touch directly.
BioTalent Ltd are acting as an employment agency in relation to this opportunity.