Descrizione:
Clinical Research Coordinator
Contract Type: Full-Time Contract (12 Months)
Key Responsibilities
- Maintain 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.
Requirements
- Previous 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.
Contact
KG Mphahlele – +44 744 134 1041
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