Roles & Responsibilities 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:
Tricia Celestine Goh (R )
Recruit Express Pte Ltd | Company Reg.
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Tell employers what skills you have Budgets
Microsoft Office
Data Analysis
Clinical Research
Ability To Work Independently
Regulatory Affairs
Healthcare
Clinical Trials
Protocol
Procurement
Medical Research
Project Management
Writing
Life Sciences
Screening
Scheduling
Terminology
Regulatory Submissions
Laboratory
IRB