Clinical Trial and Data Management Officer
Core
Coordinate and administer approved clinical trials, ensuring compliance with protocols, ethical standards, and Good Clinical Practice (GCP) guidelines while managing data collection and patient safety.
Role type
Clinical Trial and Data Management Officer
Builds
Clinical trials and research outcomes
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
GCP certification, clinical research knowledge, regulatory compliance understanding, data management, patient eligibility assessment, adverse event monitoring, clinical documentation, specimen management
Preferred skills
Postgraduate qualifications, research experience, prior clinical trial coordination in healthcare
Technologies
Clinical trial management systems (implied via data management and monitoring)
Responsibilities
Coordinate and oversee all aspects of clinical trial delivery; Assess participant eligibility and support informed consent processes; Monitor patient safety and report adverse events; Collaborate with clinicians to ensure continuity of care; Coordinate trial monitoring visits and manage clinical specimens; Maintain accurate clinical documentation and trial data
Seniority
Mid-level, hands-on operational role
