Key Responsibilities
Project Management
- Assist PI with grant funding, regulatory submissions, and IRB approvals, including correspondence with regulatory bodies and granting agencies.
 - Manage study budgets and track utilization.
 - Coordinate multi-site studies and monitor project progress.
 - Organize regular study reviews with the research team and CRU.
 - Support preparation of study-related presentations and materials.
 - Participate in evaluation and analysis of research results.
 
Study Coordination
- Perform patient screening, recruitment, and scheduling of study visits.
 - Monitor participants, ensure adherence to study protocols, and follow up as required.
 - Report adverse events, abnormalities, and protocol deviations to PI, CRU, and regulatory/ethics bodies as necessary.
 - Maintain study data integrity, accurate documentation, and compliance with ethical/regulatory guidelines.
 - Work closely with the PI and research team to ensure smooth study conduct and regular review of study data.
 
Job Requirements
- Bachelor’s degree in Life Sciences or related discipline.
 - 1–2 years of experience in a healthcare or clinical research setting preferred.
 - Proficient in Microsoft Office applications.
 - Strong written and spoken English skills.
 - Knowledge of Good Clinical Practice (GCP), clinical trials, regulatory affairs, and medical research ethics preferred.
 - Familiarity with medical and research terminology an advantage.
 - Meticulous, well-organized, and strong in coordination and administration.
 - Able to interpret, summarize, and present data clearly and accurately.
 - Strong team player with ability to work independently.
 
All qualified applicants, please send in your resume to:
triciagoh@recruitexpress.com.sg
Tricia Celestine Goh (R1981653)
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