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
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