Senior Director Clinical Research Scientist

Job description

Overview

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.

Position Overview

We are seeking a Clinical Scientist to join our Early Clinical Development Group at a level commensurate with experience (Associate Director through Executive Director).

This role is intentionally designed to attract both emerging leaders and experienced strategic contributors. Depending on level, you will contribute to or lead early clinical development and clinical pharmacology programs, with increasing ownership, strategic influence, and cross-functional leadership at more senior levels. You will have the opportunity to work across the full product lifecycle-from First-in-Human studies through approval and post-marketing-within a collaborative, science-driven environment that values curiosity, innovation, and continuous learning.

Key Responsibilities:

Core Responsibilities (All Levels)

Contribute to the design, execution, and interpretation of early clinical and clinical pharmacology studies

Collaborate cross-functionally with Clinical Operations, Translational Sciences, Quantitative Clinical Pharmacology, and Statistics

Support development of clinical documents including protocols, study reports, and regulatory submissions

Analyze and interpret clinical safety and efficacy data in collaboration with Medical and Scientific teams

Maintain awareness of competitive landscape and emerging standards of care

Ensure adherence to timelines, budgets, SOPs, and regulatory requirements

Present data internally and contribute to external scientific communications

Additional Responsibilities by Level

Associate Director Lead components of clinical studies and contribute to program-level strategy

Draft and independently own sections of key clinical and regulatory documents

Collaborate closely with cross-functional partners to execute study deliverables

Present findings to internal teams

Director / Senior Director Lead clinical studies and drive cross-functional execution

Contribute meaningfully to clinical development strategy

Serve as a scientific leader on project teams and influence decision-making

Mentor junior team members and contribute to team development

Executive Director Provide strategic leadership across programs or therapeutic areas

Shape and drive clinical development strategy and represent programs to governance bodies

Influence portfolio-level decisions and external collaborations

Serve as a recognized subject matter expert internally and externally

Lead high-visibility initiatives, including regulatory interactions and scientific presentations

Qualifications

Minimum Requirements PhD, PharmD, or MD with 5+ years of relevant experience, OR

BS/MS with 10+ years of relevant experience

Experience in early clinical development, clinical pharmacology, or a related discipline

Strong analytical, communication, and problem-solving skills

Ability to work independently and collaboratively in a dynamic environment

Additional Experience by Level

Associate Director Experience contributing to clinical studies and cross-functional teams

Demonstrated ability to analyze and interpret clinical data

Director / Senior Director Proven experience leading clinical studies or key program components

Ability to influence cross-functional teams and contribute to strategy

Executive Director Extensive experience leading clinical development programs

Strong track record of strategic leadership and influencing senior stakeholders

Experience representing programs in high-visibility settings (e.g., regulatory interactions, governance)

Preferred Qualifications (All Levels) Experience in clinical pharmacology, immunology, or oncology

Strong scientific curiosity and a proactive, question-driven mindset

Ability to present complex data clearly and effectively

Additional Information

Willingness to travel up to 20% as needed (reasonable accommodations available)

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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During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.

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You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).

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Worksite address

wilmington, DE, 19894, US

Who can apply

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