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Position Summary:

  • Review, draft, negotiate and track a variety of legal agreements.
  • Work closely with Clinical Operations study team.
  • Ensure deliverables are in alignment with defined study timelines.

Essential Functions:

  • Review, draft and negotiate a variety of agreements including master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts.
  • Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.
  • Ensure adherence to company policies, procedures and contracting standards.

Qualifications:

  • Experience in a CRO/healthcare field.
  • Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience.
  • Experienced leading interactions with Study Teams and Sponsor.

Precision for Medicine

Precision for Medicine provides biomarker-informed technology and service solutions. They aim to translate clinical findings into actionable insights that help accelerate drug development and approval, with a focus on precision medicine. They are an equal opportunity employer.

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