Clinical Research Coordinator - East Area, 5 days Office Hours #HVN

Recruit Express Pte Ltd; Singapore; On-site; SGD 30,000 - 42,000; Full time

Job summary

Recruit Express Pte Ltd in Singapore is seeking a detail-oriented coordinator to support clinical research studies. You will screen participants, coordinate visits, and ensure data integrity under the study protocols and GCP guidelines.

Ideal candidates have a life sciences or health-related degree and good communication skills. Prior healthcare or research experience is preferred, and the role involves multitasking across multiple projects and liaising with investigators and stakeholders.

Qualifications

• Degree in life sciences or related field.
• Experience in clinical research preferred.
• Strong organization and multitasking abilities.
• Good communication and interpersonal skills.

Responsibilities

• Coordinate and support clinical research studies and trials.
• Screen and recruit suitable participants according to study protocols.
• Collect, enter, and maintain accurate study data and documentation.
• Schedule study visits and liaise with investigators, patients, and stakeholders.
• Ensure compliance with study protocols, regulatory requirements, and GCP guidelines.
• Prepare reports and assist with ethics submissions and study-related administration.
• Manage research databases and maintain study records.

Skills

Organizational skills

Coordination

Communication skills

Interpersonal skills

Multitasking

Education

Life Sciences / Health-related degree

Job description

Responsibilities

• Coordinate and support clinical research studiesand trials.
• Screen and recruit suitable participantsaccording to study protocols.
• Collect, enter, and maintain accurate study dataand documentation.
• Schedule study visits and liaise withinvestigators, patients, and stakeholders.
• Ensure compliance with study protocols,regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Prepare reports and assist with ethicssubmissions and study-related administration.
• Manage research databases and maintain studyrecords.

Requirements

• Degree in Life Sciences, Biomedical Science,Nursing, Pharmacy, Public Health, or related discipline.
• Prior experience in clinical research orhealthcare setting preferred.
• Familiarity with GCP guidelines is an advantage.
• Strong organizational and coordination skills.
• Meticulous, detail-oriented, and able to managemultiple projects simultaneously.
• Good communication and interpersonal skills.