Minimum 3 years' experience in clinical trial or research setting
Strong knowledge of clinical protocols, informed consent, and trial documentation
Excellent communication, organization, and interpersonal skills
Certification in GCP (advantageous)
Coordinate and manage clinical trial activities in compliance with Good Clinical Practice (GCP) guidelines
Administer study-related procedures and medications as per protocol
Monitor patient safety, collect data, and maintain accurate documentation
Liaise with investigators, sponsors, and regulatory bodies
Ensure adherence to ethical and regulatory standards
Job Types: Part-time, Temporary
Contract length: 8 months
Work Location: In person
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