For one of our clients who have a large vaccines department, we are looking for a medical advisor.
Through interaction with internal and external stakeholdersdrive value growth of our client in Belgium and Luxembourg, using a scientific approach and taking all medical as well as compliance and regulatory aspects into account to establish the role for assigned products in the health care system.This includes not only the data on the products but also the medical environment in which the products are or could be used.
All Medical colleagues are involved in Customer-Facing Medical (CFM) interactions/activities. Customer-facing interactions are part (40 to50%) of the role of the office-based Medical colleagues.
Medical colleagues engage in non-promotional communications with Health Care Professionals (HCP) and other external stakeholders to ensure the safe and appropriate use of our medicines. Each medical visit with an external stakeholder is customized based on the careful judgment of the Medical colleague. It is important that Medical colleagues execute their activities with sound medical judgment, independence, and without actual or perceived direction by Commercial colleagues. Medical and Commercial colleagues have distinct and separate roles within our client.
Health care professionals and other relevant external stakeholders, disseminating information of medical relevance concerning the products of her responsibility and the medical implications for current practices through advisory boards, symposia and other meetings and ways of communication.
Interactions with relevant health care professionals to stimulate research efforts to establish a wider knowledge about the products and their optimal use. Actively work for initiation of Investigator Sponsored Research (ISR), Non-interventional Studies (NIS), and site selection of global company sponsored studies within the local markets.
Timely provide accurate and medically sound responses to enquiries by the medical societies and other stakeholders concerning products within her responsibility.
Ensure that marketing material is medically relevant as well as compliant with the regulatory requirements.
In collaboration with regulatory department ensure correct wording in SPC and other documents.
Provide medical/scientific expertise for formulary applications and tender processes.
Develop and maintain a strong network of Key Opinion Leaders (KOL) within the assigned therapeutic areas.
Actively participate in the Medical Affairs team and relevant meetings and projects at the EU-level in order to be updated on the current development of the therapeutic areas and influence and contribute to future development.