Associate Clinical Research Coordinator / Clinical Research Coordinator

You will be part of the research team involved in various clinical projects and will be required to perform the following:

1. Act as a liaison between study participants and the research team; provide study participants with a clear explanation of the purpose of the study and assist with obtaining informed consent.
2. Schedule participants for visits to the clinic for the required tests and evaluations, collect their samples, and assist in monitoring the participants’ well-being.
3. Assist with the compilation and management of patient data; ensure the study is conducted in compliance with study protocols, established procedures, and timeline.
4. Draft reports for submission to the relevant authorities.
5. Tabulate and document financial payments received or made to the study.

Job Requirements:

• Diploma or Bachelor’s Degree in Nursing/Medical Technology/Health Science/Life Science/Pharmacy.
• Proficient in Microsoft Office Applications.