Clinical Research Coordinator

• Be involved in subject recruitment, scheduling and data entry. Screen patients based on study eligibility, and communicate the study aims to potential subjects in layman terms.

• Obtain consent taking, administer study questionnaires and follow-up on study participants.

• Work closely with research team, clinicians, clinic staff and other relevant internal departments to ensure research study needs are met.

• Able to work on tight timelines, set sensible targets and achieve research deliverables.

Research Documentation / Administrative duties

• Conduct research study activities like patient recruitment, data collection and data management.

• Assist in data collection from electronic health records.

• Set up and maintain study investigator files, including records of consent taken and blood collection.

• Maintain study records in databases such as Redcap and in electronic health record systems.

• Responsible for maintaining strict adherence to research protocols i.e., HBRA.

• Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.

• Prepare necessary documentation for audit purposes.

• Coordinate the submission of new IRB applications, study amendments and annual reports.

• Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements and local regulations.

• Assist with any other duties of a similar nature that are delegated by the PI.