Site Contracts Manager

🔥 0 minutes ago

🌐 Serbia, Poland, +3 more countries – Remote

infoinfo

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

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Logo of Precision Medicine Group

Precision Medicine Group

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Review, draft, negotiate, and track legal agreements, including confidentiality agreements, master services agreements, clinical study agreements, site contracts, consulting agreements, vendor agreements, and amendments • Collaborate with Clinical Operations study teams, supervisors, and internal/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 policies and procedures for timely contract execution • Identify process improvements and take corrective action • 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 • Ability to handle sensitive issues with discretion • Ability to work independently and cooperatively in a virtual environment • Preferred: Bachelor’s degree in law, scientific fields, business administration, or equivalent degree • Preferred: Knowledge of setting up Contracting Plans and guides for CTA and budget negotiations

🏖️ Benefits

• Fully remote work arrangement • Equal Opportunity Employer • Reasonable accommodation for applicants with disabilities

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