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Responsibilities:

  • Review, draft, and negotiate a variety of agreements including site contracts, vendor agreements, and client contracts.
  • Resolve or escalate contractual issues with internal and external stakeholders.
  • Establish, track, and report site contract metrics.

Qualifications:

  • Minimum 5 years of experience in drafting, reviewing, and negotiating site Clinical Trial Agreements and vendor contracts.
  • Graduate degree in law, scientific fields, business administration, or equivalent.
  • CRO or healthcare experience required.

Skills and Competencies:

  • Strong organizational, written communication, and attention to detail.
  • Ability to multi-task, prioritize, and work independently in a fast-paced virtual environment.
  • Proficiency in MS Office and handling sensitive issues with discretion.

Work Environment:

  • Fully remote position based in Romania, Poland, Slovakia, Serbia, or Hungary.
  • Collaborative team environment with focus on meeting study timelines and supporting cross-functional partners.

Precision for Medicine

Precision for Medicine is a clinical research organization focused on advancing precision medicine through clinical trials and related services. It is part of the broader Precision Medicine Group, which emphasizes innovation, collaboration, and high-quality delivery.

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