Editorial summary

The company is seeking a Clinical Research Coordinator to support the execution of clinical studies, ensuring high-quality research outcomes. The role involves coordinating participant recruitment, screening, enrollment, and follow-up activities while maintaining compliance with study protocols, ethical standards, and regulatory requirements. The ideal candidate will work closely with investigators, study teams, and research participants to facilitate smooth study operations. The position offers a salary of 5,000.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/clinical-research-coordinator-drive-clinical-studies-forward-hdc1-34078 first appeared in Job-Q.com on 23 Sep 2026]

The Opportunity

Be part of a clinical research team supporting the successful execution of clinical studies and contributing to the delivery of high-quality research outcomes.

As a Clinical Research Coordinator, you will work closely with investigators, study teams and research participants to coordinate study activities from recruitment and screening through to follow-up, while ensuring adherence to study protocols, ethical standards and regulatory requirements.

Key Responsibilities

• Coordinate participant recruitment, screening, enrolment and follow-up activities in accordance with approved study protocols.

• Work closely with the Principal Investigator and study team to support study recruitment and overall site performance.

• Review study protocols, eligibility criteria and study requirements with relevant medical personnel and participants.

• Facilitate informed consent processes and ensure participant rights, safety and confidentiality are appropriately protected.

• Maintain accurate source documentation and review clinical data for completeness, consistency and accuracy.

• Complete and manage Case Report Forms (CRFs), electronic data capture systems and other study-related documentation.

• Identify missing, inconsistent or potentially inaccurate information and follow up with the relevant parties for clarification.

• Maintain essential study files, participant records, regulatory documents, consent forms, logs and study communications.

• Coordinate study supplies, including the receipt, tracking and management of investigational products where applicable.

• Monitor and document adverse events, serious adverse events, protocol deviations and other study-related issues, escalating matters when required.

• Ensure study activities and documentation are completed within required timelines and in accordance with protocol and site procedures.

• Develop study-specific documentation or source templates when required by the study.

• Communicate protocol-related matters, operational updates and study issues to the appropriate study personnel or management.

• Participate in investigator meetings, study meetings, conference calls and relevant research team meetings.

• Liaise with the Principal Investigator and research management team regarding study-specific medical or operational matters.

• Support research activities across satellite clinic sites when required.

• Uphold applicable ethical, legal, regulatory and confidentiality requirements throughout the conduct of clinical studies.

What We're Looking For

• Degree in Science, Life Sciences, Public Health, Health Sciences, Pharmacy, Medicine, Nursing or a related discipline from a recognised institution.

• Experience in clinical research, clinical trials, research coordination or a related setting is advantageous.

• Familiarity with Good Clinical Practice (GCP), clinical research regulations and ethical principles relating to human biomedical research is preferred.

• Strong organisational skills with the ability to manage multiple study activities and timelines.

• Meticulous and detail-oriented, with a strong focus on data accuracy and documentation.

• Good analytical, communication and interpersonal skills.

• Able to work effectively both independently and collaboratively within a multidisciplinary team.

Interested?

If you're keen to build your experience in clinical research and contribute to the coordination of meaningful clinical studies, we'd love to hear from you.

Please send your updated resume to  with the subject line "Clinical Research Coordinator – Leon".

EA Personnel: Leon Leong De Cong
EA Registration No.: R1551708
Recruit Express Pte Ltd
EA License No.: 99C4599

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