
Job Overview
Location
Remote, Poland
Job Type
Full-time
Category
Operations
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • Manager, Site Contracts Management role is critical to ensuring timely and efficient execution of site contracts across clinical trials, directly impacting study start-up timelines and organizational success in the European region.
- • Day-to-day responsibilities include reviewing, drafting, and negotiating clinical trial agreements and related documents; managing a team of contract and budget associates; allocating resources based on workload forecasting; ensuring adherence to company policies and contracting standards; reporting on contract metrics; and representing the organization as a Subject Matter Expert in internal and external client meetings.
- • The role sits within the Study Start Up (SSU) Leadership team at Precision Medicine Group, collaborating closely with Clinical Operations, Legal, Finance, HR, and other stakeholders to align site contracts delivery with study timelines and support strategic initiatives like the Oncology Site Network and Rapid Start-up programs.
- • The position offers the opportunity to lead process improvement initiatives, develop and implement standardized contracting procedures, gain exposure to sponsorship models and portfolio-level contract management, and grow leadership experience in a remote, cross-border European environment.
🎯 Requirements
- • 4-year college degree or equivalent experience ideally in a scientific or healthcare discipline
- • Experience in Site Contracts departments within Clinical Research Organizations (CROs)
- • Experience dealing with large healthcare institutions in North America for negotiating clinical trial agreements
- • Experience in people management, particularly in a remote work setting
- • Preferred: 5+ years of relevant experience in drafting, reviewing, and negotiating Clinical Trial Agreements and site budgets, including management and tracking at project and portfolio levels
- • Preferred: Experience in setting up Site Contracting Plans and exposure to Sponsors
🏖️ Benefits
- • Fully remote work arrangement from Poland, Slovakia, Hungary, Romania, or Serbia
- • Opportunity to participate in corporate strategic initiatives such as Oncology Site Network and Rapid Start-up programs
- • Leadership role within the Study Start Up (SSU) Leadership team with visibility across Clinical Operations, Legal, Finance, and HR
- • Professional development through process design, policy implementation, and cross-functional collaboration
- • Exposure to international contract negotiations and sponsorship models in the clinical research industry
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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