Job Description
- Assist conduct of clinical research studies and trials.
- Support clinical trials by assisting in logistical matters, preparing files/materials and arranging meetings/visits.
- Perform screening & verification activities according to protocol eligibility criteria.
- Assist investigator in explaining study objectives and procedures to potential participants.
- Comply with study protocols, applicable laws and regulations, principles, guidelines, policies and procedures.
- Interact with participants and obtain proper written informed consent from participants prior to participation in the study.
- Perform delegated protocol-specific activities completely and accurately.
- Manage data collection in an accurate and timely manner.
- Maintain research data integrity and appropriate study documentation.
- Monitor and report all adverse/ unanticipated events, abnormal results, and protocol deviations or non-compliance to appropriate parties.
- Manage applicable regulatory and ethics approvals for the assigned projects.
- Manage approved study budget including tracking the utilization of budget and financial payment.
- Participate in the evaluation of research results.
Requirements
- Minimum Diploma
- More than 1 year experience in clinical/research trails
- Prior experience in nursing background will be advantageous
- Possess knowledge of Good Clinical Practice, medical and research terminology and ethics
- Work Arrangement: 5.5 work days
- Location: Various clinics
Tng Wess Lee License No.: 02C3423 Personnel Registration No.: R1551835
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