Associate Director Pharmacovigilance

*Associate Director, Pharmacovigilance Safety Science – 12-month contract – North London/ Herts*
My client is a Global Pharmaceutical company and they have a position available for an Associate Director, Pharmacovigilance Safety Science to join their team for a 12-month initial contract.

Within this role you will be accountable for all aspects of safety science/pharmacovigilance, you will support early and late phase development activities, providing essential safety oversight and input into all aspects of study management across the entire development and marketed portfolio. In the post-market setting this may include signal evaluation, safety related activities associated with new drug applications/regulatory filings, benefit-risk assessment and safety risk management. The Associate Director will be expected to work with minimal supervision and apply strong self-leadership.

In order to apply for the Associate Director, Pharmacovigilance Safety Science contract, you should possess experience of working in the Pharmaceutical Industry in the field of pharmacovigilance with a strong knowledge of GxP and regulated processes and end to end clinical trial lifecycle. You will possess experience of writing aggregate reports and have a good knowledge of Signal management activities. You will possess excellent written and verbal communication skills and be able to communicate with health authorities and stakeholders.

Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.

To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on 0203 465 0045.

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Job type:
Working Pattern
Drug Safety and Pharmacovigilance
£65 - 75 p/h
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Talk to Roberta Atkins, the specialist consultant managing this position, located in London-City

4th Floor, 107 Cheapside

Telephone: 0203 465 0045

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