Managing participant care, ensuring protocol compliance, and upholding Good Clinical Practice standards. They lead and train clinical staff while providing direct medical care including prescribing medications, monitoring adverse events, and interpreting laboratory results. The role involves comprehensive participant assessment and follow-up, completion of case report forms (CRFs/eCRFs), response to monitoring queries, and collection of trial data. They must document all trial activities, maintain accurate records, write summary reports, and ensure the protection of participant rights while maintaining data integrity in accordance with regulations and standard operating procedures.
Bachelor’s Degree Medicine, MBChB or Bachelor of Clinical Medicine
Registration with the relevant professional body and in possession of a valid practicing license
At least 3 years work experience in Clinical trials
Flexibility in working hours when needed
Training in Good Clinical PracticeMandatory
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