Clinical Trials Site Contracts Lead

ICON Clinical Research

Paris

Sur place

EUR 70 000 - 90 000

Plein temps

Il y a 10 jours

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Avantages offerts par ce poste

Health insurance
Retirement planning
LifeWorks EAP (Global)

Résumé du poste

ICON Clinical Research seeks a Site Budget and Specialist Contract to manage the contract lifecycle from negotiation through execution and close-out. You will work with Clinical Operations, Legal and Finance to ensure timely site contracts, payments, regulatory compliance, and transparent tracking to support study milestones.

Ideal candidates hold a Bachelor's degree in a relevant field and have 2–4 years of experience in contract negotiation or clinical research, with strong GCP knowledge and

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare field.
  • 2–4 years of experience in contract negotiation or clinical research.
  • Strong understanding of clinical trial processes, regulatory requirements, and GCP.
  • Proficiency in contract management/tracking systems.
  • Excellent organizational and communication skills.

Responsabilités

  • Lead contract negotiations and ensure timely processing of site payments.
  • Ensure adherence to SOPs, regulatory requirements, and contractual commitments.
  • Identify, mitigate, and prevent contractual risks.
  • Track contract documentation and status in systems with data accuracy.
  • Provide timely status reports to study teams and stakeholders.
  • Collaborate with Clinical Operations, Legal, Finance and Management to support timelines.
  • Drive process improvements to enhance efficiency and quality.

Connaissances

Contract negotiations
Clinical research
GCP knowledge
Organizational skills
Communication

Formation

Bachelor's degree in a scientific/healthcare field

Outils

Contract management/tracking software

Description du poste

ICON Clinical Research seeks a Site Budget and Specialist Contract to manage the contract lifecycle from negotiation through execution and close-out. You will work with Clinical Operations, Legal and Finance to ensure timely site contracts, payments, regulatory compliance, and transparent tracking to support study milestones.

Ideal candidates hold a Bachelor's degree in a relevant field and have 2–4 years of experience in contract negotiation or clinical research, with strong GCP knowledge and

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