Pharmacovigilance Scientist

CK Group are recruiting for a Pharmacovigilance Scientist to join a company in the pharmaceutical sector at their site based in London on a fixed term contract basis.

Location:
The role is based at our client's site in Stratford and is easy to reach via public transport in London.

Pharmacovigilance Scientist Role:
The main purpose of the role will be to:

- Assess safety cases for seriousness and expectedness, and identify cases that require expedited reporting.
- Process Safety cases according to standard procedures and guidelines.
- Contribute to and author DSURs using SOPs and templates.

Further responsibilities will include:

- Assisting in the review of clinical trial documents, including protocols, relevant safety documents, and informed consent documents.
- Contributing to the ongoing safety evaluation process for identification of safety risks.
- Providing PV support in Safety Data reconciliation with the clinical database.

Your Background:
To succeed in this role, you will have:

- A Life Science background and previous clinical pharmacovigilance experience.
- Experience working in clinical trials.
- A working knowledge of ICH/GCP, EU pharmacovigilance legislation and clinical trial methodology.

Apply:
For more information or to apply for this Pharmacovigilance Scientist position, please contact CK Group, quoting job ref 48920.

It is essential that applicants hold entitlement to work in the UK.