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Careers At Incyte Corporation

Looking for a challenge and a chance to grow your career?

Then Incyte is the pharmaceutical company for you. While our pipeline demonstrates the ability to compete with much larger pharmaceutical companies in selecting compelling targets and creating high-quality drug candidates, our smaller size enables employees to see the direct impact of their contributions on the direction of the company. Due to our smart, agile culture and cutting-edge science, we delivered a novel, first-to-market product in an unmet medical need in 2011 - the first in the company's history.

Opportunities for taking on new and/or additional responsibilities, in addition to advancement, are a key element in our culture. Add to that a science-based, fast-paced work environment and you’ve got an exciting company in which to work.

In addition to opportunities for growth, we offer an outstanding benefits andcompensation package to help meet personal needs as well.

Take a look at our current openings to find the match that’s right for you!

Incyte Corporation values the talents of our diverse workforce and is proud to be an Equal Opportunity Employer.

Assoc Dir, Clinical Supply Operations

Department: Global IMSC
Location: Incyte Corporate Headquarters

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.

Our Global Investigation Material Supply Chain is looking for an Associate Director, Clinical Supply.  The Associate Director, Clinical Supply manages clinical supply chain of compounds in the clinical stage of development including multiple complex global studies.  The Associate Director ensures that all trials have timely and adequate supply for administration to patients.  This position drives the clinical packaging strategy for all materials needed for global clinical studies by working closely with Clinical Operations, CMC and contracted CROs and CMOs to determine manufacturing and supply needs and timelines.

Essential Functions of the Job  (Key responsibilities)

  • Act as a key interface between CMC and clinical teams.
  • Manage all aspects of clinical study requirements and Clinical Packaging activities.
  • Work with clinical operations, project management and tech ops to establish and meet timelines for clinical supplies available for clinical trials.
  • Recommend new procedures and processes to manage the growth of clinical supplies and number of clinical trials being conducted by Incyte.
  • Identify external packaging sites, monitors external clinical packaging, and reviews master and executed batch records.
  • Coordinate GMP auditing activities at CMOs, provide management with accurate time frames for resolution of delays in obtaining supplies for clinical projects, recommend insight and ideas into procedural improvements, and assist in the implementation of the improvements.
  • Work with Technical Operatons and Clinical Operations in managing inventory of clinical supplies before and during clinical studies.
  • Develop and manage strategic alliances with contract partners for procurement, packaging, transportation, brokerage, storage and distribution.
  • Develop strong internal collaboration with stakeholders, such as Clinical Operations, Regulatory Affairs, Quality, and Technical Operations functions, to ensure high customer satisfaction.

Qualifications (Minimal acceptable level of education, work experience, and competency)

  • BS or higher and minimum 7 or more years of experience in managing clinical packaging, clinical inventory and distribution.
  • Must have knowledge of US and Global clinical labeling, Ex-US depot and Qualified Person requirements for clinical supplies.
  • Work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Analytical thinker with excellent problem solving skills and the ability to adapt to changing priorities and deadlines.
  • Working knowledge of drug development process (Phase I-IV).
  • Working knowledge of cGMPs and familiarity with US and EU regulations.
  • Strong analytical and problem-solving skills.
  • Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.

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.

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