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Milestone One
Global
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.