Clinical Research Coordinator — Patient-Focused Trials

Recruit Express Pte Ltd; Singapore; On-site; SGD 47,000 - 73,000; Part time

Job summary

Recruit Express Pte Ltd is seeking a Clinical Research Coordinator to support a patient-based clinical study in a primary healthcare setting. This role blends patient interaction, study coordination, clinical research administration and stakeholder management.

The successful candidate will perform patient assessments, assist with consent and data collection, coordinate with physicians and researchers, maintain study documentation, and help ensure adherence to GCP and study protocols.

Qualifications

• Diploma or Degree in Nursing, Life Sciences, Biomedical Sciences, Pharmacy or related healthcare discipline.
• Previous experience in clinical research/coordination is compulsory.
• Knowledge of GCP and clinical protocols is preferred.
• Strong organizational and communication skills with attention to detail.

Responsibilities

• Assess patient eligibility and support recruitment.
• Obtain informed consent and conduct baseline assessments per protocol.
• Administer questionnaires and conduct follow-up calls.
• Coordinate care with physicians and allied health staff.
• Arrange appointments, labs and procedures per study requirements.
• Maintain complete research documentation and participant records.
• Track visits, reminders, and reschedule as needed.
• Manage participant reimbursements and study budget tracking.
• Assist investigators with regulatory docs and study files.
• Support recruitment and follow-up across partner sites.
• Support quality improvement and adverse-event reporting.

Skills

Clinical research coordination

Patient interaction

Healthcare administration

GCP knowledge

Education

Nursing degree

Life Sciences degree

Biomedical Sciences degree

Tools

Microsoft Office

Electronic data capture (EDC) systems

Job description

Recruit Express Pte Ltd is seeking a Clinical Research Coordinator to support a patient-based clinical study in a primary healthcare setting. This role blends patient interaction, study coordination, clinical research administration and stakeholder management.

The successful candidate will perform patient assessments, assist with consent and data collection, coordinate with physicians and researchers, maintain study documentation, and help ensure adherence to GCP and study protocols.