You will assist the Principal Investigator(s) to implement and coordinate research projects. Research project activities included screening, recruitment, events reporting, data entry, biological specimens collection and processing, maintaining of sites files, and research participants’ follow up. You will conduct phone interviews or questionnaires with the research participants. You are required to adhere to Good Clinical Practice (GCP) guideline, protocol and regulatory compliance. You will also be supporting the department with general administration. The selected candidate will be offered employment on 1 to 2-year renewable contractual terms.
Requirements:
- Degree in Science or Degree/Diploma in Nursing or its equivalent. Prior clinical research experience is not a prerequisite, though it will be an added advantage
- Proficient in Microsoft Office applications
- Proficient in English and business writing
- Good interpersonal and communication skills; and comfortable in interacting with patients
- Meticulous, a good team player, independent and self-motivated
