Research Assistant

National Healthcare Group Polyclinics; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A healthcare organization in Singapore is seeking a Project Management Coordinator to oversee and manage research projects. The role involves ensuring compliance with regulatory requirements, coordinating with research teams, managing budgets, and monitoring project progress. Ideal candidates should have project management experience, strong organizational skills, and a thorough understanding of research protocols. This position offers the opportunity to contribute meaningfully to healthcare research initiatives.

Qualifications

• Experience in managing research projects, including grants and regulatory approvals.
• Strong coordination skills to work with multiple stakeholders.
• Knowledge of regulatory and ethical requirements in research.

Responsibilities

• Oversee project management and coordination of assigned research projects.
• Assist in managing grant funding and regulatory approvals.
• Coordinate with study teams and monitor research progress.

Skills

Project management

Coordination with research teams

Monitoring and evaluation

Job description

Family Group: Administration

Job Description:

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 accordingto 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.
Becognizant 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 reportedaccordingly 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.