Clinical Trial Agreement Specialist

il y a 2 semaines


Paris, Île-de-France ICON Temps plein
Job Title: Clinical Trial Agreement Specialist

At ICON, we are seeking a highly skilled Clinical Trial Agreement Specialist to join our team. As a key member of our Clinical Contracting team, you will play a critical role in preparing, negotiating, and finalizing clinical trial agreements and budgets.

Key Responsibilities:

  • Prepare and negotiate clinical trial agreements and budgets for company-sponsored and investigator-initiated studies.
  • Work closely with the clinical team to ensure alignment with regional standards and pricing guidelines.
  • Manage the contract amendment lifecycle and track all aspects of legal documents and metrics.
  • Collaborate with global teams to review and analyze contractual terms and conditions.
  • Provide support for negotiations in confidentiality agreements, informed consent forms, and other ancillary contract documents.

Requirements:

  • ~2-4 years' experience as a Contract Specialist in the pharmaceutical industry or a CRO.
  • Excellent communication skills (both oral and written).
  • Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.).
  • Familiarity with clinical research processes.
  • Ability to work effectively in cross-functional 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 and French.

About ICON:

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology, and medical device industries. We are committed to delivering high-quality services that meet the evolving needs of our clients.



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