Coordinator
- Perform screening activities according to protocol eligibility criteria and assist in recruitment.
- Assist investigator in explaining study objectives and procedures to potential participants.
- Verify eligibility of participants before recruitment.
- Assist to obtain written consent from each study participant prior to participation in the study.
- Schedule study visits and ensure visit schedules are adhered to.
- Create source documents and any other research documents required for the successful conduct of a clinical research study or trial.
- Manage data collection in an accurate and timely manner.
- Monitor and report all adverse/ unanticipated events, abnormal results, and protocol deviations or non-compliance.
- Manage budget.
- Assist PI in preparation of study-related presentations/materials.
- Participate in the evaluation of research results where required.
Requirement
- Diploma/ Bachelor's Degree in Health Management / Nursing or equivalent
Assistant
- Conduct literature search and write up of research findings.
- Perform data collation, data cleaning, data analysis.
- Develop publication and communication plans, posters and slides for presentations as well as drafting abstracts and manuscripts for publication.
Requirement
- Bachelor's Degree in Psychology / Life Science / Public Health / Nursing or equivalent
Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button.
** We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities.**
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EA License No: 10C4754
EA Personnel: Pearly Poh
EA Personnel Reg No: R2089904
