Job Scope:
- To coordinate and assist in the conduct of clinical research studies and trials
- Perform screening activities according to protocol eligibility criteria and assist in recruitment.
- Obtain proper written informed consent from each study participant prior to participation in the study.
- Schedule study visits as per protocol and ensure visit schedules are adhered to.
- Create any documents required for the successful conduct of a clinical research study or trial.
- Assist in data collection and maintain research data integrity.
- Monitor and report all adverse/ unanticipated events, abnormal results, and protocol deviations or non-compliance to the Principal Investigator and CRU.
- Work closely with research team for smooth coordination of research projects.
- Assist PI in preparation of study-related presentations/materials.
- Ad hoc duties as assigned
Job Requirements:
- Minimum a Diploma or Degree, preferably in Life Science / Biomedical Science or equivalent
- Competent in MS Office
- Good communication and interpersonal skills
- Candidate with knowledge of Good Clinical Practice, medical and research terminology and ethics is at advantage
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 Personnel: Choong Yi Han
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