Overview
Reporting to the research team manager, you will support research studies by coordinating study activities, collecting clinical data, conducting patient interviews, ensuring proper documentation, and assisting in day-to-day study operations according to institutional and regulatory requirements.
Roles and Responsibilities
- Assist the research team in implementing research protocols and workflows
- Approach, screen, and recruit eligible patients according to study protocols
- Collect clinical data and ensure data completeness, accuracy, and confidentiality in accordance with PDPA and institutional policies
- Support preparation of study documents and assist with related administrative and logistics tasks
- Ensure all study activities comply with Institutional Review Board (IRB), institutional SOPs, Good Clinical Practice (GCP) standards, and regulatory requirements
Requirements
- Degree/Diploma in Life Sciences, Nursing, Allied Health, or related fields
- Prior research or clinical experience will be an advantage but not mandatory. Fresh graduates are welcome
- Good communication and interpersonal skills, especially with patients
- Meticulous, organised, and able to handle confidential information responsibly
- Proficient in Microsoft Office and basic data entry tools
- Ability to work independently and collaboratively in a clinical environment