Associate Director Medical Affairs - Paris, France - Regeneron Pharmaceuticals Inc.

Regeneron Pharmaceuticals Inc.
Regeneron Pharmaceuticals Inc.
Entreprise vérifiée
Paris, France

il y a 3 semaines

Sophie Dupont

Posté par:

Sophie Dupont

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Description
Our Associate Director, Medical Affairs, play a pivotal role as a professional with Oncology expertise & Scientific knowledge.

We deliver strategic and operational support by establishing, developing, maintaining scientific exchange with medical specialists, health care professionals, and payers.

We are looking for our next team member to join our Medical Affairs team in Paris.
Associate Director, Medical Affairs - Oncology
Regeneron France - Paris
Primary responsibilities of this role are to facilitate information and partake in broad scientific discussions.

This is to ensure the distribution of clinical and scientific information regarding in-development or commercialized Regeneron products in a timely, ethical and customer-focused manner.

You will work in a multifunctional, matrix organization within the medical affairs group as well as colleagues in research & development, commercial, access & reimbursement, and patient advocacy.

You will also collaborate with external partners such as health care practitioners, research groups, payers and alliance partners.


In this role, a typical day may include the following:

Participates in scientific engagement with external communities in order to educate and advance scientific and medical understanding of relevant disease areas, including the management of disease, standards of patient care, and roles of our medicines.

Builds working relationships with external partners, including patient groups and professional organizations.

Continuously maintains deep scientific and medical knowledge of relevant therapeutic area and a deep understanding of patient and physician interactions and clinical decision making and impact.

Participates in scientific engagement between Regeneron and external communities to advance scientific and medical understanding including the appropriate development and use of our medicines, the management of disease, and patient care.

Proactively brings patients' & physicians' voice from a local perspective to provide medicines meeting their needs, on cross-functional teams, while considering the needs of external collaborators, including payers.

Acts as an effective Regeneron representative interacting with external experts and attends professional/medical meetings as the in-country representative for the therapeutic area for defined products.

Collaborates to create the medical strategy and execute it with appropriate content for congresses, symposia and advisory boards and facilitates and executes such activities in country.

Delivers scientific presentations to diverse audiences (e.g. physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in meetings, advisory and/or consulting settings.
Provides medical guidance and support to the local clinical research 'field operational' team(s) where appropriate.

All activities of the Associate Medical Director are expected to be conducted in the spirit of effective cross-functional collaboration with clinical sciences and operational groups/colleagues locally and at Regeneron headquarters.

Assesses medical education needs in country and develops internal and external educational strategy as needed.

Provides appropriate medical input, while maintaining scientific integrity, to commercialization strategies in country and serves as the local medical representative at local French Commercialization teams as required.

Aids in the development and execution of an integrated strategy for optimal launch readiness, Market Access and life cycle management initiatives.

Ensures that medical input is maximised during the strategy planning.
Ensures scientific review of local promotional materials and publications in compliance with local health care laws.


This role may be for you if:
Outstanding work ethic and integrity, including high ethical and scientific standards.

You are able to work effectively in a fast-paced, rapidly changing environment and cooperatively with the team across the organization to achieve shared objectives.

You enjoy bringing new and unique ideas that move science forward and enjoy dealing with scientific concepts and complexity comfortably.

The ability to make good decisions based upon a mixture of analysis, wisdom, experience, and judgment.

The ability to make these decisions in a timely manner, sometimes with incomplete information and under tight deadlines and pressure.

Strong motivational, negotiation, listening & analytic.
You have the ability to work independently and engage in collaborative decision-making.

You ae comfortable with change & can shift gears comfortably, can decide and act without having the total picture, and can comfortably handle risk and uncertainty.

You have the ability to formally present in a variety of settings: one-on-one, in small and large groups, with peers, and supervisors.

To be considered for this role, you must have a M.D.. PhD or PharmD with expertise in Oncology disease areas. Additionally, a minimum of 10 years of e
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