Sr Site Contract Specialist
Core
Draft, negotiate, and finalize investigator contracts and grant budgets for clinical trial sites to ensure efficient site activation and compliance.
Role type
Senior Site Contract Specialist (Clinical Research)
Builds
Investigator agreements and budgetary terms for clinical trials
Domain
Pharmaceutical clinical research services
Required skills
contract law principles, investigator grant negotiation, business and financial principles, pharmaceutical product development process knowledge, CRO involvement understanding, automated systems proficiency
Preferred skills
attention to detail, analytical thinking, independent work capability, team collaboration, time management, customer-focused communication
Technologies
PPD SOP, WPDs, automated contract systems
Responsibilities
Draft, review, negotiate, and finalize agreements with study sites; negotiate investigator grant budgets and contractual terms; identify and assess legal, financial, and operational risks; coordinate with internal departments to align contract activities with site startup timelines; achieve target cycle times for site activations; escalate out-of-parameter issues per established processes.
Seniority
Senior, hands-on IC