Research Assistant

PRINCIPAL RESPONSIBILITIES
To be responsible for the project management and coordination of assigned research projects in NHGP, in accordance with the 
study protocol and applicable regulatory / ethical / institutional requirements. Where required, to participate in the evaluation of research results.

Project management:
• Assist PI in managing applicable grant funding, regulatory and IRB approvals, for the assigned projects, including 
corresponding with the granting body/ regulatory authority/ IRB.• Manage approved study budget, where applicable, including tracking the utilization of budget.
• Oversee coordination of studies with multiple sites, where applicable.
• Assist to monitor progress of study and coordinate regular reviews with the study team and CRU.
• Assist PI in preparation of study-related presentations/materials.
• Participate in the evaluation of research results where required.
Coordinate conduct of study
• Perform screening activities according to protocol eligibility criteria and assist in recruitment.
• Schedule study visits and ensure visit schedules are adhered to. Follow up and monitor participants in accordance 
with study protocol.
• Be cognizant of current regulatory, ethical and institutional requirements, and perform delegated protocol-specific 
activities according to the guidelines.
• Monitor and report all adverse/ unanticipated events and abnormalities/ protocol deviations to the Principal 
Investigator and CRU. Ensure these events are reported accordingly to granting body, regulatory authority and IRB as 
applicable.
• Maintain research data integrity and appropriate study documentation.
• Work closely with research team for smooth coordination of research projects. Meet with the Principal Investigator/ 
research team members to discuss the conduct of the study and review study data.

SECONDARY RESPONSIBILITIES
Any other duties assigned by the Reporting Officer where appropriate

Qualifications : Minimum Degree Holder in Biomedical/Health Sciences or related discipline

Experience :

• Preferably with 1-2 years of working experience in healthcare setting
• Prior experience in clinical research would be advantageous

Special Attributes and Knowledge:
• Strong interest in primary care research
• Team player with good interpersonal skills• Meticulous with good organization, coordination and administrative skills
• With good working knowledge of Microsoft Office applications
• Additional knowledge of Good Clinical Practice (GCP), medical and research 
terminology and ethics, as well as ability to use statistical programmes are preferred