Associate/Clinical Project Manager, Sponsor Dedicated
Core
Manage local clinical trials from startup to closeout, ensuring data quality, regulatory compliance, and budget adherence for assigned protocols.
Role type
Associate/Clinical Project Manager (Local Trial Management)
Builds
Local trial operations and data generation activities
Domain
Clinical Research / Life Sciences
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
Local trial management, site selection and feasibility, recruitment planning, vendor management, budget forecasting, inspection readiness, regulatory compliance (ICH-GCP), CAPA implementation, informed consent management, therapeutic area knowledge
Preferred skills
Early Phase trial experience, site visit coordination, process improvement initiatives
Technologies
CTMS, eTMF/IF, local trial management systems
Responsibilities
Oversee local trial team activities and ensure compliance with SOPs and regulations; Drive site selection and recruitment strategies; Manage local trial budget and vendor services; Ensure inspection readiness and maintain accurate trial data; Coordinate with CRA and central teams for study delivery; Prepare and manage country-specific informed consent forms; Report adverse events within required timelines.
Seniority
Associate, hands-on IC
