Site Contracts Manager

🔥 2 minutes ago

🌐 Slovakia, Poland, +3 more countries – Remote

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⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

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Logo of Precision For Medicine

Precision For Medicine

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Review, draft, negotiate, and track legal agreements, including confidentiality agreements, master services agreements, clinical study agreements, site contracts, consulting agreements, vendor agreements, amendments, and other client contracts • Resolve or escalate contractual issues with supervisors and internal/external stakeholders • Ensure compliance with company policies, procedures, and contracting standards • Update study team members on contract negotiation and execution status • Establish, track, report, and manage site contract metrics • Maintain contract files and databases, including contract archiving • Assist in designing and implementing procedures for timely contract execution • Identify process improvements and take corrective action • Collaborate with Clinical Operations study teams to align deliverables with study timelines • Perform other assigned tasks

🎯 Requirements

• Graduate, postgraduate, or 4-year college degree • Experience in a CRO/healthcare field • At least 5 years of relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, Vendor Contracts, and Site Budget negotiations • Experience leading interactions with Study Teams and Sponsors • Proficiency in MS Office software programs and computer applications • Legal authorization to work in the country of employment without employer sponsorship

🏖️ Benefits

• Fully remote work arrangement • Regular full-time employment

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