Senior Medical Director, IAI

Das ist der Job

Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.

Darum lohnt es sich

Job Summary (Primary Function) The Senior Medical Director will support the development and execution of the strategy and plans of one or more development program, in collaboration with the project team.

The employee will be an integral member of the project team and may serve as the clinical lead for individual asset(s) and/or provide critical and strategic input into the clinical aspects of late phase studies.

Experience includes a clinical leadership role on a drug development project team Self-motivation and entrepreneurial spirit Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job.

Overview A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs.

Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.

The individual will be involved with the full scope of clinical drug development activities from preclinical research through Phase 4 studies. Essential Functions Of The Job (Key Responsibilities) Identify, engage and liaise with investigators and key opinion leaders regarding program strategy and scientific advice.

Review potential in-licensing candidates and present recommendations to Senior Management groups, if requested. Support any needed due diligence and prepare/present medically sound strategy and plans associated with advanced opportunities.

Serve as an internal expert with regard to the science of the field, the competitive landscape in research, and the current state of treatment in areas of unmet medical need. Support data analysis and assembly, including clinical study report writing, contribution to the preparation of abstracts, presentations, and manuscripts.

Interpret clinical data; research, interact with and select investigators for clinical studies and post approval support (US and globally) and supply information on resource requirements to relevant groups.

Have accountability for delivery of clinical study plan along with clinical operations lead that are aligned with the clinical development plan and are ethical and consistent with standard of care and local practices.

Lead the scientific execution of global clinical studies, including the planning, design, implementation and execution of clinical programs and the design, preparation and initiation of study protocols. Contribute to the development of clinical development strategy for development assets.

Qualifications MD with advanced clinical training Minimum 5 years' experience in the pharmaceutical industry or related field Previous regulatory submission experience a plus (e.g., IND, NDA, MAA, PIP) Experience in late-stage drug development (Phase 2, 3, and 4) A credible 'thought leader' capable of inspiring others and creating a dynamic environment that fosters innovation in thought and execution, as well as transparency.

Excellent communication skills and written, verbal and presentation skills. Analytical and problem-solving skills; detailed oriented, an independent and critical thinker. Demonstrated ability to work collaboratively across all levels of the organization and to lead influentially. Strong interpersonal and negotiation skills.

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.

Pay Range USD $324,800.00 - USD $391,700.00 /Yr. #J-18808-Ljbffr