FSP Principal CTC
Core
Principal Clinical Trial Coordinator providing administrative and technical support to project teams, overseeing study administration, site activation, and regulatory compliance for clinical trials.
Role type
Senior IC clinical trial coordinator (site activation & study admin)
Builds
Clinical trial site activation and study administration processes
Domain
Life Sciences / Clinical Research
Required skills
Clinical trial coordination, site activation management, regulatory compliance, (e)TMF management, stakeholder liaison, process improvement, training delivery, data analysis, vendor management, feasibility assessment
Preferred skills
Therapeutic area expertise, strategic collaboration, system support (Activate & eTMF), global process development
Technologies
Activate, eTMF, CTMS
Responsibilities
Coordinate and oversee assigned trial activities; manage site activation critical path and site selection; maintain (e)TMF and study documentation; conduct feasibility visits and site capacity assessments; train new staff and provide technical support; liaise with local affiliates and investigators; support audit readiness and regulatory submissions.
Seniority
Senior, hands-on IC
