Site Contracts Manager

🔥 1 minute ago

🌐 Poland, Slovakia, +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 confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments • Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements and other client contracts • Collaborate with supervisors and internal and external stakeholders to resolve or escalate contractual issues • Ensure adherence to 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 improvement opportunities and take corrective action • Work with Clinical Operations study teams to align deliverables with study timelines • Perform other assigned tasks

🎯 Requirements

• Graduate, postgraduate, 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 • Ability to work independently and in a team environment • Candidates must be legally authorized to work in the country of employment without employer sponsorship • Bachelor's degree in law, scientific fields, business administration or equivalent degree preferred

🏖️ Benefits

• Fully remote work arrangement • Regular full-time employment • Equal opportunity employment • Reasonable accommodation for applicants with disabilities

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