Clinical Research CoordinatorContract Type: Full-Time Contract (12 Months)Key ResponsibilitiesMaintain and organize study files, regulatory documentation, laboratory kits, and study supplies.Coordinate and manage ordering of laboratory kits and related clinical trial materials.Prepare, package, and arrange shipment of biological samples in accordance with study and laboratory requirements.Schedule subject visits, procedures, and assessments in collaboration with investigators and site staff.Support patient visit coordination and ensure timely completion of study activities.Complete electronic Case Report Forms (eCRFs) accurately and resolve data queries in a timely manner.Assist in preparing the site for sponsor and CRO monitoring visits.Ensure study documentation is maintained in compliance with GCP, protocol requirements, and site SOPs.Support overall site operations and administrative clinical trial activities.RequirementsPrevious experience working as a Study Coordinator, Clinical Trial Coordinator, or similar clinical research role.Intermediate level clinical research experience preferred.Basic to intermediate English communication skills required.Familiarity with eCRF completion and query resolution processes.Experience handling study documentation, laboratory supplies, and sample shipments preferred.Strong organizational and multitasking abilities.Ability to work independently and collaboratively within a clinical research environment.Knowledge of GCP and clinical trial processes preferred.ContactKG Mphahlele – +44 744 134 1041
#J-18808-Ljbffr