EU Medical Advisor
EU Medical Advisor
The Medical Advisor will be a field-based role to cover regions across Europe. This is a home based role and you can be located anywhere in Europe. Regional and International travel will be required.
As a scientifically trained professional with a strong clinical background, you must have excellent communication skills. You will be responsible for liaising with leaders and healthcare professionals in academic and clinical centers for scientific exchange and data generation.
This is an exciting opportunity to be part of a passionate, high profile, high-impact Global Medical Affairs team, and work in a highly dynamic and collaborative setting.
To build and develop enduring relationships with HCPs, patient advocacy groups, professional societies and institutions, creating constructive cross-functional partnerships with internal and external stakeholders.
Contribute to the development of (and updates to) the yearly global publications plan for assigned product(s) and ensures optimal execution of plan based on regional needs.
Provide guidance in the development of strategies to demonstrate the value of disease/products within the Medical Affairs with a focus on outcomes meaningful to payer and clinical decision-makers.
Collaborate on strategy/development of materials (e.g. concept reviews) as applicable and drives toward solutions on challenging issues.
Share best practices across therapeutic areas.
Work with external vendors/service providers, including the Medical agencies of record, in assisting with medical affairs tactics including but not limited to advisory boards and medical education.
Build relationships with both internal and external global experts to drive a communication plan that advances the medical knowledge/understanding of company products and pipeline data, moves science forward, ensuring optimal benefit for patients.
Developing an expert understanding of disease state and current medical and/or regulatory issues related to company products.
Contributing to therapeutic expertise during protocol design phase.
Skills & Experience
Scientific or Medical Degree (Pharm D, PhD, MD) required.
Minimum 5 years of pharmaceutical industry experience required preferably in Oncology.
Knowledge of local pharmaceutical Code of Practice and FCPA/GPIHP, relevant SOPs.
Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
Ability to formulate (write) strategic, long-range plans that are aligned with strategies across the organization and to implement them successfully
Ability to work with multidisciplinary teams.
Excellent written, verbal and interpersonal communication skills.
Flexible, with positive attitude, strong ability to multi task, prioritize projects effectively and communicate at all levels within the company