Site Contract Specialist
Core
Prepare, negotiate, and finalize contracts with clinical study sites to ensure quality, objectivity, and risk analysis in the efficient delivery of contracts for pharmaceutical and biotech clients.
Role type
Site Contract Specialist
Builds
Investigator contracts and grant budgets for clinical trials
Domain
Pharmaceutical / Clinical Research
Required skills
Contract law principles, investigator grant negotiation, business and financial principles, French fluency, pharmaceutical product development process knowledge, CRO involvement understanding, automated systems usage
Preferred skills
Attention to detail, analytical thinking, independent work, team collaboration, time management, customer-focused communication
Technologies
Automated systems, computerized applications, PPD SOP & WPDs
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)