The main purpose of the job is to lead the UK and Ireland Medical Affairs group on the hematology portfolio, strategically and operationally. The role provides medical insights on currently marketed products and those in development with input into product launches. There are also line management responsibilities for a team of MSLs.
Duties and Responsibilities
Work cross-functionally across Medical Affairs, Market Access, Clinical Operations and the Commercial team to attain overall business goals
Lead medical affairs engagement with the UK and Ireland Market Access team with feedback of insights from customers. Support evidence generation activities and preparation of health technology submissions including PIM and EAMS.
Work with the Trials Operation Manager to ensure Incyte development clinical studies run and recruit successfully
Work with marketing colleagues to support development and approval of ABPI compliant materials and activities
Ensure UK and Ireland requirements and understood and met through participation in European working groups
Ensure effective performance management of the MSL team though appropriate objective setting with regular progress review and coaching
Develop and maintain positive relationships with Key External Experts in the allocated therapy areas, providing them with relevant medical and scientific information
Deliver scientific and medical content for medical advisory boards, as well as chairing / co-chairing, participant selection, agenda development and presentation of data
Be the point of contact for clinicians proposing investigator initiated research (IIR) in Haematology and work with investigators to ensure internal approval and timely start-up
Maintain a high level of scientific and medical knowledge in the allocated therapy areas through literature review and attendance at conferences
Conducts peer-to-peer robust scientific dialogue with external experts to generate insights regarding the place of the allocated product portfolio in a broader context
Contribute positively to a strong culture of business integrity and ethics
Act within compliance and legal requirements as well as within company guidelines
Requirements
Office based with the expectation of 3-4 days a week in Leatherhead office, 1-2 days flexible working
GMC registered physician
3-5 years pharmaceutical industry experience in Oncology Medical Affairs including ABPI final Signatory
Superior leadership skills including demonstrated ability to lead and coach scientific professionals, as well as business colleagues, at all levels of skills and knowledge
Superior interpersonal and communication skills
Ability to manage multiple projects and shifting priorities within agreed financial and resource constraints
Understanding of Haematology/Oncology drug development and approval processes, including experience designing and conducting clinical studies
Experience of interacting with NICE, SMC and AWMSG
Able to travel up to 40% of the time
Incyte is able to support continuing professional development
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
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