Manager, Clinical Site Contracting
Core
Ensuring compliant and timely execution of contracts for clinical studies, including Clinical Study Agreements (CSAs) and Master Clinical Study Agreements (MCSAs), while managing budgets and driving negotiations.
Role type
Manager, Clinical Site Contracting
Builds
Compliant clinical study contracts and budgets for pharmaceutical research
Domain
Pharmaceutical industry, Clinical Research Operations
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Contract negotiation, Clinical study lifecycle knowledge, Budget management, Team leadership, Process improvement, Regulatory compliance understanding, Cross-functional collaboration, SOP development, Stakeholder management, Risk mitigation
Preferred skills
Advanced degree, Global environment experience, Project management, Conflict resolution, Multitasking
Technologies
Contract management systems, Legal templates
Responsibilities
Execute clinical study contracts (CSAs, MCSAs, CDAs) ensuring compliance and fair market value; Lead and develop a team of up to 5 direct reports; Manage internal and external relationships with investigational sites and legal teams; Develop SOPs, job aides, and training tools; Drive cross-functional process improvement initiatives; Negotiate terms and manage cost drivers associated with clinical agreements.
Seniority
Manager, direct line management