What are the responsibilities and job description for the Executive Director, Clinical and Quantitative Pharmacology position at Incyte Corporation?
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 Executive Director, Clinical and Quantitative Pharmacology is responsible for all aspects of clinical drug development and is expected to play a key role in supporting all programs. This role will be responsible for developing and implementing model-informed drug development (MIDD) strategies to optimize decision-making across all phases of drug development. The Executive Director will provide strategic leadership, mentor a team of pharmacometricians, and collaborate cross-functionally to advance our portfolio of innovative therapeutics.
Essential Functions of the Job (Key responsibilities)
- Define and execute the pharmacometric strategy for drug development programs, ensuring alignment with regulatory expectations and industry best practices.
- Provide scientific leadership in model-based approaches, including population PK/PD, exposure-response modeling, disease progression modeling, and clinical trial simulation.
- Partner with Clinical Pharmacology, Translational Medicine, Biostatistics, Regulatory, and Clinical Development teams to integrate quantitative methodologies into development strategies.
- Ensure effective resource allocation and prioritization across multiple projects in alignment with company goals.
- Champion model-informed drug development (MIDD) strategies to improve decision-making across discovery, clinical development, and regulatory submissions.
- Lead the preparation and review of pharmacometric contributions to regulatory submissions, responses, and meetings with global health authorities.
- Drive innovation by identifying emerging trends, tools, and methodologies in pharmacometrics and their application to drug development.
Qualifications (Minimal acceptable level of education, work experience, and competency)
- Ph.D. in in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, Engineering, or a related field.
- 12 years of related industry experience.
- Proven experience in leading and managing scientific teams
- Excellent communication skills and ability to effectively collaborate with cross-fucntional teams and influence decision-making process.
- Ability to balance execution of multiple tasks to accomplish program goals.
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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