Overview
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In this role you will review, draft, and negotiate a range of agreements to support clinical studies. You will collaborate with the Clinical Operations team to ensure contracts align with study timelines and milestones. You help optimize contract processes and maintain accurate contract files and metrics. The position offers remote work from several European countries and contributes to reliable study execution and sponsor relationships. This is an impactful role for someone who thrives in a fast-paced, cross-functional setting and wants to shape contracting practices in a clinical research environment.
Responsabilidades
Review, draft, and negotiate site contracts, master service agreements, confidentiality agreements, vendor and consulting agreements
Collaborate with study teams and stakeholders to resolve contractual issues
Ensure adherence to contracting standards and company policies
Provide status updates on contract negotiations and execution to the study team




Establish and report contract metrics; maintain contract files and archiving
Design and implement policies to speed up contract execution; identify process improvements
Perform other duties as assigned
Requisitos principales
Minimum 4-year degree (graduate/postgraduate acceptable)
Experience in CRO/healthcare with drafting, reviewing, and negotiating site CTAs, vendor contracts, and site budget negotiations (≥5 years)
Experience leading interactions xqbhyrx with study teams and sponsors
Strong organizational and communication skills; attention to detail
Knowledge of contracting plans and CTA/budget negotiations
Ability to manage relationships with study teams/CRAs and meet timelines
excellent organizational and written communication
attention to detail
self-motivated and able to work independently
professionalism and reliable commitments
MS Office proficiency
contracting plans and negotiation frameworks

📌 Site Contracts Manager (Murcia)
🏢 Precision For Medicine
📍 Murcia