Job Description
- Assist in the management, logistics and operations of research programs
- Collaborate with stakeholders to ensure project milestones and completion with stipulated timeframes
- Coordinate and execute project plans, manage timelines, track project performance and deliverables and budget
- Responsible for research and grant administration activities and budget utilization and control
- Organize events related to the research programme
- Coordinate the planning and execution of associated initiatives and publicity plans separately or in conjunction with other major events
- Assist in regulatory and IRB approvals for the research projects under the research programme(s), where necessary
- Assist in preparation of relevant reports/ presentations/ materials
- Assist in supervising staff involved in data collection and data entry/ transcription
Requirements
- Bachelor degree in Life Science or related discipline
- Minimum 5 years of experience in supervisory, operations and administrative work in a healthcare organization
- Experience in clinical research and research regulatory affairs.
- Knowledgeable in Good Clinical Practice, research ethics, clinical trials and regulatory affairs.
- Comfortable with 1 year renewable contract
- Location: Buona Vista
Tng Wess Lee License No.: 02C3423 Personnel Registration No.: R1551835
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