The Associate Clinical Research Coordinator provides research support service for clinical or health services research, in accordance with applicable regulatory, Good Clinical Practice and protocol requirements. He/she works closely with the Principal Investigator (PI), members of the department, study sponsors and monitors, etc. to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical studies.
Responsibilities
- Act as a liaison between study participants and the research team provide study participants with clear explanation of purpose of study and assist with obtaining informed consent
- Schedule participants for visits to clinic for the required tests and evaluations, collect their samples and assist in monitoring the participants well-being
- Assist with compilation and management of patient data ensure study is conducted in compliance with study protocols, established procedures and timeline
- Draft reports for submission to the relevant authorities
- Tabulate and document financial payments received or made to the study
- Other ad hoc duties as assigned
Job Requirements:
- Diploma/Adv Diploma in Nursing (on project basis), Diploma in Life Science/Pharmaceutical Science/ Clinical Trial Management
- Knowledge of MS Office software
