Job Description:
The Clinical Trials Coordinator oversees the daily operations of clinical research studies, ensuring that trials are conducted efficiently, ethically, and in full compliance with regulatory guidelines. The coordinator is responsible for patient recruitment and follow-up, scheduling study visits, handling regulatory submissions, managing documentation, and maintaining data quality.
In collaboration with investigators and sponsors, the coordinator prepares ethics committee submissions, tracks protocol amendments, manages study supplies, and ensures timely data entry into clinical databases. This role requires frequent interaction with patients, healthcare providers, CROs, and clinical staff, and contributes directly to the smooth execution of multi-phase clinical trials.
The Clinical Trials Coordinator is key to ensuring the logistical and operational success of trials. The role demands excellent organizational skills, attention to detail, and the ability to balance patient care with research requirements.
Job Requirement:
Candidates must have a degree in biomedical sciences, healthcare management, or nursing, with 3–5 years of experience coordinating clinical studies or patient-facing trials. Familiarity with IRB processes, informed consent, GCP guidelines, and trial documentation is essential. Applicants should possess strong communication, multitasking, and database management skills. Proficiency in Microsoft Office and clinical software (CTMS, EDC) is expected. Fluency in English is required; Arabic is an asset. Clinical trial certification or training is preferred.
