Research Asst
- Study Coordination: Screen, recruit, and schedule eligible patients for clinical trials and research studies.
- Data Management: Collect, clean, enter, and validate clinical data for downstream statistical analysis.
- Regulatory Compliance: Prepare Institutional Review Board (IRB) applications and maintain essential trial documentation, ensuring full audit readiness.
- Administrative Duties: Assist Principal Investigators with literature reviews, grant preparation, and drafting manuscripts for peer-reviewed medical journals.
- Patient Communication: Educate research participants about study protocols, risks, and benefits while maintaining good rapport.
Requirements
- Bachelor’s Degree in Biomedical Science or equivalent;
- Working experience in academic or clinical research would be advantageous;
- Proficient in MS Word, MS Excel, Power Point and Outlook;
- Good written and oral communication skills;
- Team-oriented with strong coordination and organisational skills;
- Able to work independently and comfortable to multi-task / handle a few projects concurrently