FSP Site Contract Specialist
Core
Prepare, negotiate, and finalize investigator contracts and grant budgets with clinical study sites to ensure efficient site activation and compliance.
Role type
Site Contract Specialist (Clinical Trials)
Builds
Investigator agreements and budgetary terms for clinical trials
Domain
Pharmaceutical/CRO industry, Clinical Research
Required skills
Contract law principles, Investigator grant negotiation, Budgetary guidance, Risk analysis, Contractual process compliance, Pharmaceutical product development process knowledge
Preferred skills
English and Polish language proficiency, Automated systems usage, Customer-focused communication
Technologies
PPD SOP & WPDs, Automated systems, Computerized applications
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 site startup activities with contractual timelines; Achieve target cycle times for site activations.
Seniority
Mid-level (2-5 years experience)