at Incyte Corporation in Wilmington, Delaware, United States
Job Description
Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.
The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.
Job Summary (Primary function)
The Sr. Medical Director, Vitiligo is responsible for programs and deliverables through partnership with Medical Science Liaisons, Scientific Communications, Publications, Clinical Development, and the Commercial Team. The incumbent is accountable for high quality execution of Medical Affairs activities including establishing and maintaining key partnerships and collaborations, and support of relationships with external experts, both directly, and in conjunction with, the Medical Science Liaison team.
Essential Functions of the Job (Key responsibilities)
Provide support for planning and execution of the Medical Affairs program strategy for vitiligo.
Expertly deliver scientific and medical information and interpretation of clinical research findings.
Serve as medical leader and subject matter expert in dermatology/vitiligo.
Provide medical expertise in a cross-functional environment to field based medical science liaisons as well as internal stakeholders (Medical Affairs functions, Marketing Department, Clinical Development, Clinical Operations, Regulatory Affairs, Biostatistics, and Drug Safety/ Pharmacovigilance Department, Sales Training).
Participate in the design, conduct, analysis, and reporting of Medical Affairs led clinical trials and observational studies.
Provide medical review and expertise and serve as medical monitor for independent investigator-sponsored research (IIR).
Provide Medical expertise to the Commercial organization, including review of promotional materials, sales training, and speaker training for promotional programs.
Interface with external experts and health care professionals at major medical conferences, advisory boards, and other external meetings.
Provision of medical/scientific expertise for relevant marketing materials (including all promotional material) copy review in the Medical-Legal-Regulatory (MLR) Committee.
Interact with the Global and EU Medical Affairs function at Novartis, our partner for activities outside of the U.S.
Develop, track, execute and report on goals and objectives.
Be accountable for compliant business practices.
Qualifications (Minimal acceptable level of education, work experience, and competency)
M.D. degree required.
Board Certified or Board Eligible status in dermatology, or allergy and immunology, or Internal Medicine (equivalent foreign certification accepted).
Pharmaceutical industry work experience of at least five (5) years highly preferred. Minimum of 2 years of direct Medical Affairs experience.
Experience with new product launch, preferably in dermatology and autoimmunity is highly desirable.
Experience in atopic dermatitis and vitiligo is a plus.
Experience as either Medical Monitor for Industry-sponsored studies or (principal or associate) Clinical Investigator in academia.
Medical Affairs, Understanding of Clinical Development and Commercial activities is preferred.
Ability to partner effectively with Field Medical staff is required.
Strong clinical insight, understanding of translational medicine and knowledge of clinical trials, including registries, and successful prior experience in the management of an IIR portfolio.
Strong business acumen, vision and perspective.
Ability to comprehend and combine complex sets of data.
Ability to educate internal stakeholders on disease state and/or product/ brand-specific information.
Ability to present and discuss complex clinical, medical, biological, or translational data.
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.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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