Feasibility Study Manager
Core
Coordinate and manage site feasibility activities throughout the clinical trial study lifecycle, focusing on electronic survey preparation, launch, monitoring, and closure to identify suitable clinical trial sites.
Role type
Clinical research operations manager (site feasibility)
Builds
Clinical trial site identification pipelines and feasibility data
Domain
Clinical research / Pharmaceutical / Biotechnology
Required skills
Electronic survey platform configuration, survey branching and conditional logic, data quality assurance, investigator information management, CDA coordination, survey reporting, risk monitoring, site identification strategy execution, communication planning, survey lifecycle management
Preferred skills
Clinical trial operations experience, site identification experience, investigator engagement experience, knowledge of CDAs
Technologies
Electronic survey platforms, survey management systems
Responsibilities
Adapt draft site feasibility questionnaires into electronic survey platforms; Configure survey branching, conditional logic, and scoring parameters; Develop and maintain survey reporting templates; Conduct quality checks on potential investigators and clinical trial sites; Upload identified site lists into the survey management system; Coordinate survey launches and oversee ongoing preparation and monitoring; Manage survey delegation and reconcile survey statuses; Identify and investigate invalid or missing investigator contact details; Monitor and report country-level survey responses and identify risks; Execute agreed site identification strategies; Implement communication strategies and coordinate supporting materials; Coordinate revisions to survey content and site lists; Monitor the progress of site CDA negotiations; Manage survey closure activities; Maintain accurate survey records
Seniority
Mid-level, hands-on IC