Site Activation Manager
Core
Manage site activation project management and delivery activities, overseeing site identification, contract status, and document collection to ensure study start-up within assigned therapeutic areas.
Role type
Site Activation Manager
Builds
Clinical trial study start-up and site qualification
Domain
Clinical Research / CRO
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Project management, site identification, contract management, risk assessment, budget management, SOP development, process improvement, metric analysis, proposal support
Preferred skills
Feasibility support, site selection, business development, training and coaching
Technologies
MS-Office (Word, Excel, PowerPoint), digital clinical systems
Responsibilities
Serve as primary point of accountability for study start-up and maintenance; oversee functional groups to ensure critical path activities are completed on-time and within budget; compile, manage, track, and analyze site activation activities; support feasibility and site identification; expedite Site Qualification and Selection; communicate project status to Sponsor and project team; prepare risk assessment and mitigation plans; ensure study activities are present in work order budgets; develop and maintain site activation project plans; contribute to SOP development and process improvement; establish and interpret site activation metrics; participate in business development proposals and bid defense meetings; report and escalate issues to ensure resolution.
Seniority
Mid-level, hands-on IC
