Clinical Trials Coordinator
Core
Coordinate clinical studies and trials from start-up to close-out, ensuring protocol and documentation compliance for patients and staff.
Role type
Clinical Trials Coordinator
Builds
Clinical research studies in dermatology
Domain
Healthcare / Dermatology / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial coordination, ICH-GCP knowledge, regulatory compliance, participant recruitment, study documentation management, ethics submissions, investigational product accountability
Preferred skills
Health-related degree, multidisciplinary team collaboration, project management, communication
Responsibilities
Coordinate and manage assigned clinical trials from study start up through to study close out; Facilitate clinical trials in accordance with study protocols, ICH-GCP and regulatory requirements; Act as the primary site contact for Sponsors, CROs and Clinical Research Associates; Coordinate participant recruitment activities and maintain screening and enrolment logs; Develop and manage study documentation and maintain accurate trial records within approved research systems; Prepare Ethics and Local Governance submissions and amendments; Manage investigational product accountability and study-related documentation; Collaborate with Investigators, Sponsors and the Clinical Trials team to ensure successful study delivery; Maintain compliance with quality, safety and infection prevention standards.