CY Partners have a fantastic opening, for a Medical Director, to join a world leading global pharmaceutical organisation. The role is available as a remote working opportunity, with an opportunity to work from their site in London, a few days per week, if office working is a preference.

As a Medical Director, you will have the opportunity to provide high level medical expertise in the day-to-day safety evaluation and risk management of key HIV assets in the post-marketing setting.

As part of a skilled team of physicians and scientists, you will be conducting routine pharmacovigilance activities, signal detection/evaluation, authoring and reviewing key regulatory documents (e.g., DSURs, EU RMPs and PBRERs), identifying the need for product labelling updates, and driving proactive implementation of risk management initiatives.

The role will also involve ensuring that adverse event and other safety information is efficiently evaluated and accurate in order to meet global compliance and regulatory requirements. Alongside, leading presentation of safety-related findings and data to senior stakeholders and governance boards.

For this role, candidates must be GMC registered and should also have drug Safety/ Pharmacovigilance experience from within the pharmaceutical industry. HIV experience is not essential.

For an informal confidential discussion about the role, please contact Helen Tomlinson at CY Partners on 07851246847 or apply by email with an up-to-date CV to [email protected]

Tagged as: drug safety, DSURs, EU RMPs, GMC registration, medical affairs, Medical Director, PBRERs, pharmacovigilance, Physician