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Pharmacovigilance Director

Central London   •  Negotiable  •  Permanent, Full time

Pharmacovigilance Director

A position has arose, to work with a global pharmaceutical company. This is a fantastic opportunity to be part of a well-funded business to grow this is a truly exciting time to join the company.

With their growth plans, they are looking for a Pharmacovigilance Director which will be a part of the Global Safety Department, frequently collaborating with other safety staff and other groups such as clinical development and regulatory affairs, and working within a fast paced environment.

Responsibilities, though not limited to:

• Conducting routine pharmacovigilance activities, signal detection/evaluation and leading authoring of key regulatory documents (e.g. DSURs, EU RMPs and PBRERs).

• Leading the monitoring and evaluation of safety data.

• Ensuring studies are designed and delivered with a focus on the safety of participants and safety objectives.

• Ensuring that all safety documentation is accurate and available to meet global compliance and regulatory requirements.


• Significant experience with Safety Evaluation and Risk Management.

• Relevant degree/high-level degree qualification.

• Experience of international pharmacovigilance requirements such as ICH, GVP modules, CIOMS initiatives.

• Experience with drug development and approval processes.

If you are interested in growing your professional career please send your CV to Selina.Watson@cpl.com or call 0118 959 4990 for a confidential discussion.

  • Agency: Cpl Life Sciences
  • Reference: JO-2309-522754
  • Posted: 14th September 2023
  • Expires: 12th October 2023

Cpl Life Sciences

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