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 [email protected] 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