Responsibilities
- Conduct subject recruitment, screening, scheduling, and data entry based on study eligibility criteria.
- Communicate study objectives clearly to participants using layman terms and obtain informed consent.
- Administer study questionnaires and manage follow-up with participants.
- Collaborate with clinicians, clinic staff, and internal departments to meet research study requirements.
- Perform data collection from electronic health records and maintain accurate study documentation.
- Manage study investigator files, including consent forms and biological sample records.
- Maintain databases such as Redcap and electronic health record systems with high accuracy.
- Ensure strict adherence to research protocols including compliance with HBRA guidelines.
- Coordinate clinical workflows across multiple departments for recruitment activities.
- Prepare documentation for audits and support IRB submissions, amendments, and annual reports.
- Uphold professional conduct and record-keeping standards in line with hospital policies and ethics regulations.
Requirements
- Bachelor’s degree in Science, Public Health, or Social Science.
- Candidates with no experience are welcome to apply; training will be provided.
- Strong interpersonal and communication skills with a high sense of accountability.
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:
EA Personnel Name: Felicia Chiam Kar Min
EA Personnel Reg.
No.: R
EA Licence No.: 07C5771
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