Responsible for implementing study activities in strict adherence to the study protocol, including participant recruitment, screening, and informed consent.
Diploma in Clinical Medicine and Surgery, Nursing, or Medical Laboratory Sciences from a recognized institution.
A valid practicing license where applicable.
Additional training in research ethics is an advantage.
Prior research experience is an added advantage.
Ability to multitask, solve problems, and collaborate effectively to resolve challenges.
Strong communication and organizational skills.
Excellent interpersonal and written communication skills.
Capacity to maintain a high level of confidentiality when handling participant records.
The ability to ride a motorbike, with a valid riding license, is an added advantage.
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