Clinical Research Coordinator - East Area, 5 days Office Hours

Recruit Express Pte Ltd; Singapore; On-site; SGD 40,000 - 70,000; Full time

Job summary

Recruit Express Pte Ltd in Singapore is seeking a Clinical Research Coordinator to support studies and trials from protocol to data management.

You will screen and recruit suitable participants, coordinate study visits, and maintain accurate study data and documentation, ensuring compliance with GCP and regulatory requirements. The role demands meticulous, detail-oriented multitasking and clear communication with investigators, patients and stakeholders.

Qualifications

• Degree in Life Sciences, Biomedical Science, Nursing, Pharmacy, Public Health, or related discipline.
• Prior experience in clinical research or healthcare setting preferred.
• Familiarity with GCP guidelines is an advantage.

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 withinvestigators, patients, and stakeholders.
• Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (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

Education

Degree in Life Sciences, Biomedical Science, Nursing, Pharmacy, Public Health, or related discipline

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.