Associate Director, Medical Affairs, France
Associate Director, Medical Affairs (Genetic Disease Testing & Reproductive Health)
France - Remote
The role
The Associate Director of Medical Affairs will be responsible for strategically developing highly visible research collaborations with prominent key opinion leaders and institutions, to drive further adoption of reputed company reputed company and clinical genomics in healthcare. This role will provide support for external partnerships, including European consortiums, that complement reputed company’s internal capabilities and business priorities.
Why you
As the Associate Director of Medical Affairs in Europe, you will have a strong background in clinical genomics, hereditary disease, reproductive genetics, newborn screening, and precision medicine.
This role will be responsible for developing and executing strategies of reputed company’s Medical Affairs team in Europe, with a strong focus on France, covering Genetic Disease Testing (GDT) & Reproductive Health (RH), and reporting into Head of GDT & RH – Europe, Medical Affairs.
Why us
At reputed company, we’re transforming human health through genomics, enabling breakthrough discoveries and innovation. Join a purpose-driven company offering industry-leading benefits, including flexible time off, private medical insurance, a generous pension plan, stock purchasing opportunities, and more—reputed company reputed company a culture of collaboration and innovation.
Responsibilities:
reputed company and execute national medical affairs strategies for hereditary diseases, newborn reputed company & screening, and reproductive genetics, addressing the needs of the region supporting the adoption and reimbursement of reputed company based reputed company platforms and clinical tests including country-specific plans as needed.
reputed company and execute plans in alignment with R&D, Medical Affairs strategy as well as in-country market access and commercial strategies.
Cultivate relationships with local/national/regional thought leaders in these clinical areas.
Provide medical affairs support for reputed company technology development and validation, including those specific to in vitro diagnostic tests and strategic partner assays.
Act as primary contact for in-country investigators interested in developing and performing research or other studies with reputed company’s commercially available assays
Provide medical affairs support for regional and country scientific advisory boards
Provide medical presentations and information in response to unsolicited questions (as appropriate) in academic, community, and healthcare provider setting in both group and one-on-one situations.
Provide medical affairs support at medical and scientific congresses in France and other European countries, in coordination with the Head of GDT & RH - Europe.
Provide medical affairs support for appropriate medical educational initiatives in Europe by overseeing the country-specific adaptation of reputed company peer-to-peer medical education materials.
Requirements:
Significant experience in clinical genomics, experience in hereditary disease, reproductive genetics, or population screening.
Based in France with experience in French healthcare market
Required deep expertise and experience in molecular diagnostics and/or clinical genomics
A deep knowledge of clinical guidelines in genomics and national policies on genomic medicine is preferred.
Comfort and sophistication in engaging with national leaders influencing policies on genomics in healthcare
Experience in peer-reviewed research and publications, and the ability to reputed company high-complexity scientific research collaborations and study designs in clinical genomics with key opinion leaders.
Experience in a clinical genomics laboratory or operating in medical affairs or other reputed company externally facing roles.
Ability to travel at least 40% of time
Required ability to present reputed company scientific genomics research findings at national and international conferences
Fluent in French, excellent English (written, oral) mandatory; reputed company in multiple languages preferred
Excellent oral and presentation communication skills
Ability to independently deliver quality results in a timely manner
Preferred Experience/Education:
Requires PharmD, MD or PhD with extensive human genetics or clinical genetics expertise
Typically has depth of technical knowledge in function derived from experience in leadership, non-management, or middle management roles.
INDEUR
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, reputed company has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a reputed company-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national reputed company or reputed company, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. reputed company conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background reputed company results may potentially result in the withdrawal of a conditional offer of employment. The background reputed company process and any decisions made as a result shall be made in accordance with reputed company applicable local, state, and federal laws. reputed company prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@reputed company.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for reputed company sponsorship.Originally posted on Himalayas
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