Editorial summary

The company is seeking a Clinical Research Coordinator to support the execution of high-quality clinical studies, ensuring compliance with safety, ethical, and regulatory standards. The role involves coordinating daily operations, including participant recruitment, screening, enrollment, follow-up visits, and retention activities. Candidates should have relevant experience in clinical research and possess strong organizational skills. The position offers a salary of 6,000.

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

Job description

[This job id 23005 first appeared in Job-Q.com on 02 Aug 2026]

Join a collaborative clinical research team and play an important role in advancing healthcare through high-quality clinical studies. This is an excellent opportunity to work alongside investigators and healthcare professionals while ensuring research is conducted safely, ethically, and in accordance with regulatory standards.

Key Responsibilities

• Coordinate the day-to-day operations of clinical research studies from participant recruitment through study completion.
• Support participant screening, enrolment, scheduling, follow-up visits, and retention activities in accordance with study protocols.
• Guide participants through study procedures, eligibility requirements, and informed consent processes.
• Work closely with investigators and multidisciplinary research teams to ensure smooth study execution and achievement of research milestones.
• Maintain compliance with study protocols, Good Clinical Practice (GCP), regulatory requirements, and ethical guidelines.
• Accurately collect, review, and enter clinical data into electronic research systems while ensuring data quality and integrity.
• Prepare, organise, and maintain study documents, regulatory files, and essential research records.
• Monitor study timelines, protocol compliance, adverse events, and follow up on required actions where necessary.
• Coordinate study supplies, research materials, and investigational products when applicable.
• Liaise with internal stakeholders, sponsors, and research partners to facilitate efficient study operations.
• Participate in research meetings, site discussions, and study-related activities.
• Safeguard participant confidentiality and uphold the highest standards of research ethics and professionalism.

Requirements

• Degree in Science, Life Sciences, Public Health, Health Sciences, Pharmacy, Medicine, Nursing, or related disciplines and above.
• Experience in clinical research, clinical trial coordination, research administration, or a healthcare-related environment will be an advantage.
• Knowledge of Good Clinical Practice (GCP), clinical research regulations, and ethical guidelines is preferred.
• Meticulous with strong organisational, analytical, and problem-solving skills.
• Able to manage multiple priorities effectively in a dynamic environment.
• Strong communication and interpersonal skills with the ability to work collaboratively across multidisciplinary teams.

Interested applicants are invited to send their updated resume to with the subject title "Clinical Research Coordinator".

We regret that only shortlisted applicants will be notified.

Leon Leong De Cong
R1551708
Recruit Express Pte Ltd
EA Licence No. 99C4599

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