Senior Clinical Development Scientist, Early Development

Incyte; Wilmington (DE); On-site; USD 150,000 - 230,000; Full time

Job summary

Incyte is seeking a Clinical Scientist to join our Early Clinical Development Group in Delaware. The role supports designs and execution of early clinical and clinical pharmacology studies, with increasing ownership at Associate Director through Executive Director levels.

You will collaborate across Clinical Operations, Translational Sciences, and Statistics, contribute to regulatory documents, interpret safety and efficacy data, and help shape development strategies across product lifecycles.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Early clinical development

Clinical pharmacology

Cross-functional collaboration

Data interpretation

Communication skills

Education

PhD/MD/PharmD

BS/MS with 10+ years

Job description

Incyte is seeking a Clinical Scientist to join our Early Clinical Development Group in Delaware. The role supports designs and execution of early clinical and clinical pharmacology studies, with increasing ownership at Associate Director through Executive Director levels.

You will collaborate across Clinical Operations, Translational Sciences, and Statistics, contribute to regulatory documents, interpret safety and efficacy data, and help shape development strategies across product lifecycles.