This is a full-time, on-site role for a Clinical Research Associate based in Durban. The Clinical Research Associate will oversee the daily operations of clinical trials, ensure compliance with protocols, and manage research activities. Responsibilities include coordinating with clinical trial sites, monitoring the progress of studies, and maintaining accurate documentation. The role involves close collaboration with other clinical research professionals to ensure the integrity and quality of the research data.
Responsibilities:
Assume the role of regional monitor for all trials conducted in the VM-CTU for an estimated 5 trials per annum.
Develop and maintain Standard Operating Procedures relevant to the portfolio.
Create trial monitoring plans in conjunction with the trial sponsor representatives.
Conduct study initiation visits for each new trial protocol to assess site readiness for study activation.
Conduct trial monitoring (clinic, laboratory and pharmacy) to ensure compliance with study protocols, SOPs, ICH-GCP, and local regulatory requirements.
Review case report forms (CRFs), source documents, and data entry to verify accuracy, completeness, and timeliness.
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