Clinical Contracts Specialist

il y a 5 jours


Paris, Île-de-France Parexel Temps plein

About the Role:

Parexel FSP is seeking an experienced Investigator Contracts Lead to join our team in France.

Job Summary:

The Investigator Contracts Lead will be responsible for negotiating and managing contracts with clinical investigator sites, including initial agreements and amendments. This role will also involve managing the Per-Subject Cost (PSC) process for assigned studies and collaborating with other teams to plan site contracting timelines.

Key Responsibilities:

  • Develop and negotiate global clinical study agreements with institutions and investigators participating in sponsored clinical trials.
  • Work with partners to develop and oversee the global site budget process.
  • Negotiate cost, business, and contractual terms and conditions with investigators/institutions.
  • Lead study-level site contracting activities and act as primary study point of contact for site contracting issues and timelines.
  • Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space.
  • Collaborate with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements.

Requirements:

  • Balance of general business, compliance, finance, legal, and drug development experience.
  • Precise communications and presentation skills.
  • Ability to plan, identify, and mitigate risks to site contacting timelines.
  • Ability to lead by influence rather than positional power to accomplish critical deliverables.
  • Success in working in a highly matrix-based organization.
  • Fluency in written and spoken French is required.
  • Advanced level of English, written and spoken.
  • Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities.

Education:

  • Bachelor's Degree or equivalent and 5+ years of experience in clinical development operations or clinical trial outsourcing OR PhD/Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing.


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