Director, Clinical Research Scientist IAI
Incyte
8 days ago
Remote friendly (Wilmington, DE)
United States
Clinical Research and Development
Job Summary
The clinical scientist will provide scientific clinical and operational input to early and late-stage clinical development programs, working on cross-functional teams to design, execute, and monitor clinical trials, and assisting with data interpretation and communication.
Key Responsibilities
- Develop protocols for clinical studies.
- Contribute to program strategy for assigned compounds/programs, including participation in clinical development plans.
- Draft and review clinical scientific documents (e.g., IND amendments, Investigator Brochures, Annual Reports, and other Health Authority submissions).
- Monitor, review, and summarize safety and efficacy data in ongoing studies.
- Represent clinical development on project teams.
- Develop relationships with consultants and external experts to obtain feedback on protocol design.
- Serve as clinical lead for study abstracts, posters, oral presentations, and manuscripts.
- Act as liaison to project teams, CROs, clinical sub-teams, and others.
- Maintain awareness of competitive landscape (assets with similar MOA and/or evolving standards of care).
Qualifications
- Degree in scientific/life-sciences; Pharm.D. or Ph.D. preferred.
- Minimum 5 years of drug development experience (alternative experience considered).
- Prior Dermatology or immunology experience preferred.
- Ability to work independently, multi-task, and thrive in a fast-paced environment.
- Excellent written and oral communication skills.
- Strong analytical ability.
- Ability to accommodate up to 20% travel or as business dictates.
The clinical scientist will provide scientific clinical and operational input to early and late-stage clinical development programs, working on cross-functional teams to design, execute, and monitor clinical trials, and assisting with data interpretation and communication.
Key Responsibilities
- Develop protocols for clinical studies.
- Contribute to program strategy for assigned compounds/programs, including participation in clinical development plans.
- Draft and review clinical scientific documents (e.g., IND amendments, Investigator Brochures, Annual Reports, and other Health Authority submissions).
- Monitor, review, and summarize safety and efficacy data in ongoing studies.
- Represent clinical development on project teams.
- Develop relationships with consultants and external experts to obtain feedback on protocol design.
- Serve as clinical lead for study abstracts, posters, oral presentations, and manuscripts.
- Act as liaison to project teams, CROs, clinical sub-teams, and others.
- Maintain awareness of competitive landscape (assets with similar MOA and/or evolving standards of care).
Qualifications
- Degree in scientific/life-sciences; Pharm.D. or Ph.D. preferred.
- Minimum 5 years of drug development experience (alternative experience considered).
- Prior Dermatology or immunology experience preferred.
- Ability to work independently, multi-task, and thrive in a fast-paced environment.
- Excellent written and oral communication skills.
- Strong analytical ability.
- Ability to accommodate up to 20% travel or as business dictates.