Site Contract Specialist-II / Contract Manager II (Sponsor Dedicated
Core
Managing clinical site contracts, budgets, and lifecycle activities to support efficient clinical trial start-up and site activation.
Role type
Senior IC clinical contract specialist
Builds
Clinical Trial Agreements, site budgets, and start-up documentation for pharmaceutical sponsors
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical Trial Agreement (CTA) negotiation, site budget management, contract lifecycle administration, Phase II–IV trial knowledge, ICH-GCP principles, project management, risk identification
Preferred skills
Sponsor-Dedicated/FSP model experience, CRO experience, process improvement initiatives
Technologies
Microsoft Office Suite, Sponsor clinical trial tracking systems
Responsibilities
Independently manage CTAs, amendments, and site budgets; draft and negotiate contract language using approved templates; maintain internal project trackers and clinical trial systems; prepare and lead study kick-off meetings; identify contractual and operational risks; prepare contract and budget escalations.
Seniority
Mid-level, hands-on IC
