Incyte

Senior Director, Clinical Research Scientist

Incyte$150K — $180K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Willingness to travel up to 20%, with accommodations for disabilities.
  • Strong analytical skills enhanced through practical experience.
  • Excellent written and verbal communication capabilities.
  • Proven ability to work independently and manage multiple tasks.
  • Experience in oncology drug development preferred but not mandatory.
  • Several years of research experience in relevant drug development processes required.
  • Degree in scientific/life-sciences field or equivalent experience; advanced degrees valued.

Responsibilities

  • Maintain knowledge of competitive landscape and evolving standards of care.
  • Serve as liaison to project teams and CROs, facilitating communication and project progress.
  • Lead clinical aspects of study abstracts, posters, and manuscripts, ensuring diversity is represented.
  • Build and leverage relationships with consultants and external experts for protocol design feedback.
  • Represent clinical development on project teams, contributing insights and expertise.
  • Monitor and summarize safety and efficacy data from ongoing studies.
  • Contribute to program strategy and development by drafting clinical scientific documents and protocols.

Benefits

  • Opportunity to work on cutting-edge clinical research in a supportive team environment.
  • A chance to collaborate with leading professionals in the healthcare field.
  • Support for professional growth through relationships with external experts and consultants.
  • Flexible travel options with accommodations for diverse needs.
  • Engagement in diverse and inclusive representation in clinical materials.
Full Job Description
Overview

This position is responsible for working with the physicians within Clinical Development to provide clinical research support for programs as assigned by phase or therapeutic area.

Essential Functions of the Job (Key responsibilities)
• Maintain updated knowledge of competitive landscape in regard to assets with similar MOA and/or evolving standards of care for indications of interest.
• Serve as liaison to project teams, CRO's, Clinical sub-teams, and others.
• Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned studies, ensuring inclusive and diverse representation in all materials.
• Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.
• Represent clinical development on project teams.
• Monitor, review and summarize safety and efficacy data in ongoing 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.
• Development of protocols for clinical studies.

Qualifications (Minimal acceptable level of education, work experience, and competency)
• Willingness to travel up to 20% or as business needs require, with accommodations available for individuals with disabilities.
• Strong analytical skills.
• Strong written and verbal communication skills.
• Ability to work independently, manage multiple priorities, and thrive in a dynamic environment.
• Experience in oncology drug development is preferred, but not required, to encourage candidates from diverse backgrounds to apply.
• Minimum of several years of experience in research with relevant drug development experience are required. Alternative drug development experience will be considered.
• Degree in scientific/life-sciences field or equivalent experience. Advanced degrees such as Pharm.D. or Ph.D. are valued but not required.

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.

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About Incyte

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of proprietary therapeutics. The company was founded in 1991 and is headquartered in Wilmington, Delaware. Incyte's main focus is on oncology, inflammation, and autoimmunity. The company's flagship product, Jakafi, is a JAK1/JAK2 inhibitor used to treat myelofibrosis and polycythemia vera. Incyte has a number of other products in development, including itacitinib, a JAK1 inhibitor for the treatment of graft-versus-host disease, and pemigatinib, a FGFR inhibitor for the treatment of cholangiocarcinoma.
Learn more about Incyte
Size
2,094 employees
Market Cap
$17.6 billion
Industry
Net Income
-$295.7 million
Founded
1991
5 Year Trend
+22%
Revenue
$2.6 billion
NASDAQ

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