Clinical Trial Site Agreement Specialist

hace 4 semanas


Madrid, Madrid, España Precision Medicine Group A tiempo completo
Job Title: Clinical Trial Site Agreement Specialist

We are seeking an experienced Clinical Trial Site Agreement Specialist to join our European team. The ideal candidate will have strong experience in Clinical Site Agreements across Europe, with a focus on managing site agreements across multiple European countries.

Key Responsibilities:
  • Review, draft, negotiate, and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements.
  • Develop and implement contracting strategies for assigned projects, working closely with the Clinical Operations study team.
  • Negotiate site budgets and ensure deliverables are in alignment with defined study timelines.
Requirements:
  • Minimum 4 years of experience in setting up contracting strategy, drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budget negotiation.
  • Strong organizational and communication skills, with attention to detail and ability to multi-task in a fast-paced environment.
  • Experience interacting with Global institutions, with a main focus on European ones.
What We Offer:
  • A dynamic and collaborative work environment.
  • Opportunities for professional growth and development.
  • A competitive salary and benefits package.

Precision Medicine Group is an Equal Opportunity Employer. We are committed to diversity and inclusion in the workplace. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please contact us at hr@precisionmedicinegroup.com.



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