Director, Clinical Research Scientist IAI

Biopharma Careers; Wilmington (DE); In loco; USD 120.000 - 180.000; Tempo pieno

Descrizione del lavoro

Incyte Corporation is seeking a Clinical Scientist to provide scientific, clinical, and operational input across early and late-stage development programs. You will join cross-functional study teams to design, execute, and monitor trials and assist with data interpretation and communication.

The role involves drafting regulatory documents, leading study abstracts and presentations, and collaborating with CROs and internal teams. Travel up to 20% may be required.

Competenze

• Degree in scientific or life-sciences field; Pharm.D. or Ph.D. preferred.
• Minimum 5 years of drug development experience.
• Dermatology or immunology experience preferred.

Mansioni

• Develop protocols for clinical studies and contribute to program strategy.
• Draft and review clinical documents (IND amendments, Investigator Brochures, annual reports).
• Monitor safety and efficacy data in ongoing studies and summarize findings.

Conoscenze

Excellent communication

Analytical ability

Independent multi-tasking

Formazione

Degree in scientific/life-sciences

Pharm.D. or Ph.D. preferred

Descrizione del lavoro

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.

Key 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 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, CROs, Clinical sub-teams and others.
• Maintain updated knowledge of competitive landscape in regard to assets with similar MOA and/or evolving standards of care for indications of interest.

Qualifications

• Degree in scientific/life-sciences. Pharm.D. or Ph.D. preferred.
• Minimum of 5 years of drug development experience are required.
• Alternative drug development experience will be considered.
• Prior Dermatology or immunology experience is preferred.
• 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

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.

We Respect Your Privacy Learn more at: http://www.incyte.com/privacy-policy The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate. 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. You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. 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). Please contact [e-mail] if you have any questions or concerns or would like to exercise your rights.