
Clinical Study Professional
2 weeks ago
Clinical Research Coordinators play a vital role in Human Biomedical Research studies.
Key Responsibilities- Recruit and screen patients based on study eligibility, explaining the study aims to potential subjects
- Obtain consent, administer questionnaires, and follow-up with study participants
- Collaborate with research teams, clinicians, and staff to ensure research needs are met
- Work efficiently, set targets, and achieve research deliverables
- Conduct patient recruitment, data collection, and management activities
- Assist in collecting data from electronic health records
- Maintain investigator files, records of consent taken, and blood collection
- Manage study records in databases like Redcap and electronic health record systems
- Adhere strictly to research protocols
- Liaise with investigators, clinicians, and laboratory teams to establish clinical workflows
- Prepare documentation for audits
- Coordinate IRB applications, study amendments, and annual reports
- Maintain high standards of professional conduct and record-keeping
- Bachelor's degree in Science, Public Health, or Social Science with 2 years of relevant experience
- Fresh graduates welcome
- Strong interpersonal and communication skills, with leadership desirable
- Independent, mature, and able to work in a team
- Meticulous, organized, and able to multitask
- Ability to work in an interdisciplinary environment
- Bilingual preferred
- Willingness to travel between hospitals and external sites
Candidates should be familiar with Good Clinical Practice guidelines and the Human Biomedical Research Act.
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