The Clinical Research Coordinator I/II provides research support service for clinical or health services research, in accordance with the 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. In addition, he/she ensures smooth and efficient day-to-day logistics support for research and innovation projects and assists in study quality control activities such as internal monitoring and prepares for auditing/ inspection. The Clinical Research Coordinator supports and participates in the SGH Nursing Research and Innovation mission of providing quality patient care, education, research.

• Manages research study independently. Acts as liaison between subjects and other members of the research team to facilitates and coordinates the daily research study activities.
• Participates in the evaluating of the study proposals and protocols. Comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
• Assists in budget preparation and facilitates clinical trial agreement discussion.
• .Provides study protocol specific training to delegated staff with supervision of PI.
• Provides on-job-training for new CRC/ACRC.
• Assists in Quality Control & Quality Assurance activities, such as department study internal monitoring and department audit/ inspection.

Requirements

• Bachelor Degree in Life Science/ Pharmacy & any other relevant disciplines, or Diploma in Life /Pharmaceutical Science/Clinical Trial Management, Diploma /Advance Diploma/ Degree in Nursing
• Knowledge of MS Office software
• Prior working experience in healthcare setting preferred
• Have experience managing and coordinating multiple projects