Job Scope:
• Coordinate and support the execution of clinical research studies and trials.
• Conduct screening activities following protocol eligibility criteria and contribute to participant recruitment.
• Secure proper written informed consent from each study participant before their involvement.
• Schedule study visits per protocol, ensuring adherence to timelines.
• Generate necessary documents essential for the successful conduct of clinical research studies or trials.
• Assist in data collection and uphold research data integrity.
• Monitor and promptly report adverse events, unanticipated occurrences, abnormal results, and protocol deviations or non-compliance to the Principal Investigator and CRU.
• Collaborate closely with the research team to ensure the seamless coordination of research projects.
• Assist the Principal Investigator in preparing study-related presentations and materials.
• Undertake ad hoc duties as assigned.
Requirements:
- Diploma or Degree Holder
- Experienced in research trails and with nursing background will be an advantage.
- Good communication and interpersonal skills
- Proficient with MS Office applications
- Ability to work independently and commit 5.5 days work-week.
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.**
JOBSTUDIO PTE LTD
EA License No: 10C4754
EA Personnel: Hiew Qing Hua
EA Personnel Reg No: R23114639
