The Drive to Discover. The Experience to Deliver.

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.


Study Start Up Specialist

Department: Development Operations
Location: Incyte Corporate Headquarters

Study Start Up Specialist

This position performs assigned activities within the Clinical Trial Logistics Study Start-up team (CTL SSU). Responsibilities include but are not limited to: providing support to CTL SSU; creating/managing relationships with investigative sites while building efficiencies across various Incyte clinical trial programs to effectively start the clinical programs.  This employee will work in our Wilmington, DE corporate office.

Job Responsibilities

  • Assist in the development and negotiation of Master Clinical Trial Agreements (MCTAs) and site budget rate cards with investigative sites;
  • Oversee essential documents collection, tracking and review to support the activation of sites across multiple studies
  • Serve as a site liaison, identify and build efficiencies across various Incyte clinical trial programs;
  • Develop and manage a site intelligence repository in the CTL SSU tool; enables team members to track and update activities within the tool
  • Provide support to CTL SSU as needed including liaising with sites to negotiate contracts and budgets and collection of essential regulatory documents;
  • Develop metric dashboards and report quarterly metrics and KPIs;
  • Manage repository of site start up processes (institutional and investigators) to maintain consistency in start-up processes; and
  • Maintain consistent communications with internal clients, and study team members to expedite site activation.

 

Minimum Requirements

  • Bachelorís Degree in business administration, finance, science or related field;
  • Minimum of five years of relevant experience in the biopharmaceutical/CRO industry; and
  • Minimum of five years negotiating US Site contracts and budgets
  • Excellent negotiation skills;
  • Experience with conflict resolution;
  • Proven ability to effectively manage change;
  • Experience with review and collection of essential documents required for site initiation;
  • History of establishing relationships with sites;
  • Ability to negotiate complex contract and payment terms;
  • Flexibility to assume a workload which frequently necessitates an adjustment of priorities;
  • Goal oriented, self-starter with proven ability to work independently;
  • Able to proactively identify issues and provide potential solutions for resolution;
  • Detail oriented;
  • Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines;
  • Proficiency with Grant Plan and all applications of Microsoft Office;
  • Preferred experience with Veeva Vault;
  • Good interpersonal skills; and
  • Comfortable with ambiguity; ability to act without having the total picture

 

 

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