Clinical Research Coordinator

National Healthcare Group Polyclinics; Singapore; On-site; SGD 40,000 - 70,000; Full time

Job summary

A healthcare organization in Singapore is seeking a Clinical Research Coordinator to assist in conducting research studies according to protocols and regulations. The role involves recruiting participants, managing data collection, and ensuring compliance with regulations. Ideal candidates should have experience in clinical research, strong organizational and communication skills. This position offers an opportunity to contribute to impactful healthcare research efforts.

Qualifications

• Experience in clinical research or similar field.
• Strong communication skills for participant interaction.
• Organizational skills to manage multiple tasks and priorities.

Responsibilities

• Coordinate clinical research studies and trials.
• Recruit participants and explain study objectives.
• Perform data collection and ensure research integrity.
• Manage regulatory and ethics approvals.
• Oversee study budgets and logistical arrangements.

Job description

Family Group: Ancillary

To coordinate and assist in the conduct of clinical research studies and trials in NHGP in compliance with study protocols, applicable laws and regulations, principles, guidelines, policies and procedures.

Responsibilities

• 1. Perform screening activities according to protocol eligibility criteria and assist in recruitment. Assist investigator in explaining study objectives and procedures to potential participants. Verify eligibility of participants before recruitment.
• 2. Obtain or assist to obtain proper written informed consent from each study participant prior to participation in the study. Interact with participants to ensure study compliance.
• 3. Perform delegated protocol-specific activities completely and accurately. Schedule study visits as per protocol and ensure visit schedules are adhered to. Follow up and monitor participants in accordance with study protocol.
• 4. Create source documents and any other research documents required for the successful conduct of a clinical research study or trial.
• 5. Manage data collection in an accurate and timely manner. Obtain all necessary documentation as required by the protocol and perform data entry, including updating of various study-specific tracking logs. Maintain research data integrity and appropriate study documentation.
• 6. Monitor and report all adverse/unanticipated events, abnormal results, and protocol deviations or non-compliance to the Principal Investigator and CRU. Ensure these events are reported accordingly to funding agencies, regulatory authority and ethics committee as applicable.
• 7. Coordinate and facilitate monitoring visits and/or audits. Assist PI in appropriate follow-up actions arising from the monitoring visits and/or audits.
• 8. Work closely with research team for smooth coordination of research projects. Provide timely updates on study progress with study team members. Meet with the Principal Investigator and research team members regularly to discuss the conduct of the study and review study data.

Additional Administrative Duties

• Where applicable, assist PI in managing applicable regulatory and ethics approvals for the assigned projects, including drafting correspondences with the regulatory authority and/or ethics committee.
• Coordinate with study team, CRU and clinics to start up study site(s) in NHGP, including making necessary logistical arrangements, setting up investigator files, preparation for study initiation meetings/visits.
• Manage approved study budget, where applicable, including tracking the utilization of budget and financial payment.
• Oversee coordination of studies with multiple sites and collaborators, 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.