Clinical Research Coordinator
2 weeks ago
Our client in the healthcare industry is looking to hire Clinical Research Coordinators (CRC) to assist in a Human Biomedical Research study. As a CRC, you will be primarily responsible for subject recruitment and other research deliverables for the studies, and work closely with the research team and Principal Investigator.
Responsibilities- 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.
- 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.
- Bachelor Degree in Science/ Public Health/ Social Science with 2 years relevant experience
- Fresh graduates are welcome to apply.
- Able to adapt in a fast-paced environment, with a strong focus to meet research deliverables and targets.
- Strong interpersonal and communication skills. Leadership and accountability to tasks is very desirable.
- Independent and mature. Able to work independently, as well as in a team.
- Meticulous, well-organized and able to multi-task
- Ability to work in an interdisciplinary environment with different groups of stakeholders.
- Bilingual preferred (fluent in Mandarin/Malay/Tamil).
- Willing to travel between the Hospitals and external study sites as part of his / her work.
- Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM, are required.
- Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)
Interested candidates, please click “Apply Now” or send your resume to
We regret that only shortlisted candidates will be notified.
Felicia Lua Wei Xuan | CEI Reg. No.: R
Job Lions Pte Ltd | EA Licence No.: 21C0594
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