Job Overview:
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.
Job 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:
- Diploma in Life Sciences, Nursing, Allied Health, or related fields.
- Prior research or clinical experience will be an advantage but not mandatory.
- 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.
