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Role and Responsibilities:

  • Review, draft, and negotiate a variety of legal agreements including confidentiality agreements and clinical study agreements.
  • Establish process and procedures for overall site contract management within the organization.
  • Escalate and resolve complex issues with clients and internal stakeholders.

Qualifications and Experience:

  • Graduate degree and 7+ years of experience in drafting and negotiating site clinical trial agreements.
  • CRO experience required, with oncology experience preferred.
  • Strong organizational and communication skills with attention to detail.

Work Environment:

  • This is a fully remote position based in Hungary, Poland, Romania, Serbia, or United Kingdom.
  • Ability to work independently and collaboratively in a virtual environment.
  • Demonstrates professionalism, sound business judgment, and proactive work style.

Precision for Medicine

Precision for Medicine is a life sciences company that provides clinical research services. They are an established organization with a focus on supporting clinical trials and employ a global team with a culture of collaboration and professionalism.

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