Director / Senior Director, Clinical Research Scientist

InCyte•Wilmington, DE

59d

About The Position

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. Job Summary The clinical scientist will provide scientific, clinical, and operational input to early and late stage clinical development programs. This role will work on cross-functional study teams for the design, execution, and monitoring of clinical trials, as well as assist with data interpretation and communication.

Requirements

Degree in scientific/life-sciences field.
Minimum of 5 years of drug development experience are required.
Alternative drug development experience will be considered.
Ability to work independently, multi-task, and work 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

Nice To Haves

Pharm.D. or Ph.D. preferred.
Prior Dermatology or immunology experience is preferred.

Responsibilities

Development of protocols for clinical studies.
Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans
Drafting and review of clinical scientific documents such as IND, 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 appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.
Clinical lead for study abstracts, posters, oral presentations and manuscripts for assigned studies.
Serve as liaison to project teams, CRO's, Clinical sub-teams, and others.
Maintain updated knowledge of competitive landscape in regards to assets with similar MOA and/or evolving standards of care for indications of interest.

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume