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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.