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Job Details

Contracts & Grants Analyst

Company: inVentiv Health Clinical
Reference: IH/6114
Closing Date: 23 Nov 17
Type: Full Time
Salary (£): On Application

Job Summary:

Are you ready to work alongside the brightest minds at INC Research/inVentiv Health?


Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose:  shortening the distance from lab to life.  You’ll work alongside the brightest minds to create better, faster, smarter processes to speed therapies to patients that need them the most.  In fact, in a recent five-year period, INC Research/inVentiv Health has helped to develop or commercialize at least 82% of novel new drugs approved by the FDA and at least 70% of products granted marketing authorization by the EMA.



At this moment we are looking for a


Contracts & Grants Analyst


to work solely for one of our clients, one of the major pharmaceutical players in the world. The role can be partially home-based and office-based in Beerse, Belgium or Breda, The Netherlands.


Your responsibilities will be as follows:


  • Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations. Responsible for delivery on established targets/measurements.
  • Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.
  • Participate in discussions related to the development of site/investigator budgets aligned with fair market value.
  • Manage the contract amendment lifecycle.
  • Work with the global C&G team as necessary to review and analyze contractual terms to reach resolution. Assess risks of budget and legal provisions in conjunction with members of the C&G team and support functions. Escalate issues as appropriate.
  • Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.
  • Assume responsibility for all aspects of legal document and metrics tracking.
  • Provide support to review, authorize and/or understand aspects of site payments. Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.



The ideal candidate has:

  • A bachelor’s degree
  • 3 year’s experience and/or equivalent competencies in legal/pharmaceutical industry/clinical research
  • Excellent communication skills
  • Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.) a plus
  • Familiarity with clinical research processes a plus
  • Ability to work effectively in cross function teams
  • Strong and proven negotiation and problem resolution skills
  • Working knowledge of PCs (MS Office suite at a minimum) and database management
  • Fluency in English is required
  • Must demonstrate innovative spirit, have strong interpersonal skills, and ability to manage a high volume of work
  • Previous experience working in virtual teams preferred



How to apply?

Are you ready to work alongside the brightest minds at INC Research/inVentiv Health? In this role you’ll be fully employed by INC Research/inVentiv Health and will enjoy our very competitive primary and secondary benefits. Please contact Eveline Wigtman or Irene Houtsma via  with reference to job number 6114.

Apply for this job: Contracts & Grants Analyst

Contact Information:

Address:  France
41 rue des trois Fontanot
92 000 Nanterre

Reasons to work for inVentiv Health Clinical
Website:  Visit Our Web Site

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