FSP Principal Clinical Trial Coordinator - Bulgaria
Core
Coordinate and facilitate project activities as a study lead, acting as a cross-functional liaison to support rapid site activations and oversee administration on assigned clinical trials.
Role type
Principal Clinical Trial Coordinator (Site Activation & Feasibility)
Builds
Clinical trial site activation plans, feasibility assessments, and regulatory compliance documentation for pharmaceutical/biotech clients.
Domain
Clinical Research / Life Sciences
Required skills
Site feasibility assessment, regulatory document review, stakeholder liaison, process improvement, training delivery, data reconciliation, vendor management, site selection strategy, audit readiness support, critical path planning
Preferred skills
Therapeutic area expertise, local market knowledge, system administration (eTMF/CTMS), strategic collaboration
Technologies
eTMF, CTMS, Activate, various tracking systems
Responsibilities
Coordinate site activation critical path and feasibility visits; review local regulatory documents and Investigator files; train new staff and provide technical support; liaise with global teams and local affiliates; manage vendor trackers and site lists; support audit responses and document transmission; conduct phone interviews with investigators for protocol optimization.
Seniority
Principal, hands-on IC with mentorship responsibilities