Medical & Scientific Advisor

Description:

Are you interested in a medical affairs role that leverages your project management expertise to accelerate medical affairs engagement? If so, this Medical and Scientific Advisor role could be an ideal opportunity to explore.

As a Medical and Scientific Advisor and acting as a Final Medical Signatory, you will play a pivotal role in safeguarding the integrity of our medical content and materials. Working within a dynamic and collaborative environment, you will have the opportunity to collaborate with cross-functional teams to ensure that our communications adhere to regulatory guidelines while effectively conveying the benefits and risks of our products.

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.

In this role you will

 

• Uphold the highest compliance standards & provide authoritative opinion on medical and ethical matters to support colleagues across GSK, enabling the evidence- based use of GSK medicines and compliance with the relevant statutory requirements (e.g. ABPI Code of Practice, Medicines Act, and EU Directives).
• Responsible for conducting medical review and ABPI Code signatory examination and certification of materials
• Writing of GSK’s response to complaints from bodies such as the PMCPA or MHRA – this will typically involve engaging with members of the extended brand team e.g. brand manager, regulatory affairs manager.
• Provide leadership, advice and coaching on how to work compliantly in the execution of UK Pharma Digital Engagement initiatives in order to deliver UK Digital Driven customer experience (DDCx ).
• Support creation & delivery of the Medical Digital & Technology plan for Omnichannel.
• Act as formal mentor & coach to new signatories/signatories in training. - if on approved UK list
• Lead, or provide input into, updating and or development of SOPs