The Clinical Research Coordinator functions as part of the research team involved in various clinical research projects.
You will act as liaison between subjects and members of the research team, obtaining relevant information by interviewing subjects and explaining aims and plan of the project in layman terms, address their concerns and questions and arranging for their informed consent.
You will schedule subjects for visits to clinic for the required tests and evaluations; Collect their samples and assist the investigators in monitoring the subjects’ well-being.
You will have to ensure compliance with protocols and schedules of evaluation, compile relevant patient data and maintain proper documentation.
You will provides study protocol specific training to delegated staff and provide on-job-training for new junior staff. You will assist in Quality Control & Quality Assurance activities, such as department study internal monitoring and department audit/ inspection.
You will assists study sponsor or Principal Investigator in the study submission to IRB or HSA; oversee all study subject-related issues, timely report all safety events according to sponsor, IRB and regulatory authorities requirements.
Job Requirements :
- Bachelor’s Degree in Nursing/ Medical Technology / Health Science / Life Science / Pharmacy with relevant academic certification
- Minimum 2 years of relevant experience
- Knowledge of MS office software
- Bilingual and/or knowledge of local dialects desired
