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Clinical Research Co-ordinator job at NHG Health, Singapore | WorkJio
Full-time Healthcare & care · Posted 7 Sept
Clinical Research Co-ordinator N NHG Health From company site
Salary
Not stated by the company
Start Not stated
Work mode On-site
Experience Experienced About the role This role supports the conduct of clinical research studies and trials across NHG Polyclinics, working within a research team and alongside principal investigators. It suits someone organised and detail-minded who can follow study protocols closely and communicate well with participants and colleagues.
What you'll do Screen potential participants against protocol eligibility criteria and help with recruitment Support investigators in explaining study objectives and procedures to participants Confirm participant eligibility before recruitment Obtain or help obtain written informed consent before participation Keep in touch with participants to support study compliance Carry out delegated protocol-specific activities completely and accurately Know someone for this? Share it
Schedule study visits according to protocol and ensure schedules are followed
Follow up and monitor participants in line with the study protocol
Create source documents and other research documents needed for studies
Collect data accurately and on time, complete data entry and maintain tracking logs
Keep research data integrity and study documentation in order
Monitor and report adverse or unanticipated events, abnormal results and protocol deviations to the Principal Investigator and CRU
Report such events to funding agencies, regulatory authorities and ethics committees where applicable
Coordinate and facilitate monitoring visits and audits, and help with follow-up actions
Work with the research team to keep projects coordinated and share progress updates
Meet regularly with the Principal Investigator and team to discuss study conduct and review data
Help manage regulatory and ethics approvals, including drafting correspondence
Assist with administrative aspects and overall coordination of assigned projects
Coordinate with the study team, CRU and clinics to start up study sites, including logistics, investigator files and initiation meetings
Track approved study budget utilisation and financial payments where applicable
Oversee coordination of multi-site studies and collaborations where applicable
Help monitor study progress and coordinate regular reviews
Assist the Principal Investigator in preparing study-related presentations and materials
Take part in evaluating research results where required Good to know Based in Singapore, working with NHG Polyclinics Requirements Able to follow study protocols, laws, regulations, guidelines and SOPs Comfortable interacting with study participants Accurate and timely with data collection and entry Able to maintain research data integrity and documentation Willing to report adverse events, abnormal results and protocol deviations Able to coordinate monitoring visits and audits Apply on the company website
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Open application Listing ID 5627 · Report this listing
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