Overview In this role you will review, draft, and negotiate site contracts and related agreements to support clinical trials. You will collaborate with Clinical Operations to align contracting deliverables with study timelines and maintain contract records. You will contribute to developing policies that speed up contract execution and improve process efficiency, all while managing stakeholder communications in a remote environment.
Responsabilidades Review, draft and negotiate a variety of agreements including site contracts, master confidentiality agreements, consulting agreements, vendor agreements, and other client contracts
Collaborate with study teams and sponsor to resolve contractual issues and keep stakeholders informed on status
Ensure adherence to company contracting policies and standards
Update study team members on contract negotiation/execution progress
Establish, track, and report site contract metrics; maintain contract files and databases




Assist in designing and implementing policies to enable timely contract execution; identify and implement process improvements
Handle additional tasks as assigned
Requisitos principales Minimum of 5 years' experience in drafting, reviewing and negotiating site CTAs, vendor contracts, and site budget negotiations in a CRO/healthcare setting
Experience leading interactions with study teams and sponsors
Knowledge of contracting plans and guides for CTA and budget negotiations (preferred)
Excellent organizational and communication skills with attention to detail
Proficiency in MS Office; ability to work independently and in a virtual environment
strong organizational skills
excellent written and verbal communication
attention to detail
self-motivation and ability to work independently
professionalism and good interpersonal skills
MS Office

📌 Site Contracts Director (Toledo)
🏢 Precision For Medicine
📍 Toledo