
Clinical Research Coordinator West
4 days ago
[Job ID: ]
Responsibilities:
- Recruit and screen study participants based on eligibility criteria.
- Communicate study objectives clearly to participants in layman terms.
- Obtain informed consent and administer study questionnaires.
- Schedule participant visits and manage follow-up activities.
- Collaborate with clinicians, research staff, and internal departments to meet study goals.
- Collect and manage data from electronic health records and study databases (e.g., Redcap).
- Maintain accurate and organized study documentation, including consent forms and sample records.
- Ensure compliance with research protocols and regulatory requirements (e.g., HBRA).
- Coordinate IRB submissions, amendments, and annual reports.
- Support clinical workflow setup across multiple departments for recruitment.
- Prepare documentation for audits and maintain high standards of professional conduct.
Requirements:
- Bachelor's degree in Science, Public Health, or Social Science.
- No experience candidates are welcome to apply; training will be provided.
- Familiarity with Good Clinical Practice (GCP) guidelines and Human Biomedical Research Act (HBRA) is an added advantage.
We regret that only shortlisted candidates will be notified. However, rest assured that all applications will be updated to our resume bank for future opportunities.
Please kindly refer to the Privacy Policy of Good Job Creations for your reference:
If you are interested in the role, please kindly email your updated resume to
EA Personnel Name:Felicia Chiam Kar Min
EA Personnel Reg. No.:R
EA Licence No.: 07C5771
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