Site Contracts Manager

📋 Description

• Oversee negotiation process for clinical study agreements on assigned trials.
• Plan CSA execution strategy aligned with start-up delivery and client expectations.
• Prepare CSA templates, payment terms, and country budgets with stakeholders.
• Lead CSA negotiations and finalize/execute CSAs per timelines.
• Negotiate with sites in assigned countries; escalate out-of-parameter requests.
• Provide consultation during escalation of budget/contractual queries.

🎯 Requirements

• BS degree in law, business, life sciences or related field.
• Strong CRO operational experience in Site Contracts Management at local/regional/global level.
• Thorough knowledge of regulations, drug development and clinical project management.
• Understanding of country requirements for Site Contracts in own country and ability to work across
• Mentoring skills, strong presentation and interpersonal abilities; proficient in MS Office.
• Ability to manage multiple tasks, meet deadlines, and communicate effectively.

🎁 Benefits

• Collaborative, international team with focus on work-life balance.
• Purpose-driven work in rare disease and oncology trials.
• Opportunities for professional growth and ownership in projects.