Clinical Research Coordinator | Drive Patient-Centered Trials

NATIONAL UNIVERSITY HOSPITAL (SINGAPORE) PTE LTD; Singapore; Presencial; SGD 40.000 - 67.000; Tempo integral

Resumo da vaga

The National University Hospital (NUH) is seeking a Clinical Research Coordinator to support a range of studies from screening and recruitment to data collection and regulatory compliance. You will work with Principal Investigators, clinicians, sponsors, and regulatory bodies to ensure adherence to GCP and institutional policies.

Responsibilities include coordinating participant visits, collecting data, assisting with informed consent, and supporting study materials and dissemination of

Qualificações

• Bachelor's degree in health-related science or related field is required.
• At least 2 years of clinical research coordination experience preferred.
• Knowledge of ICH-GCP guidelines and local regulatory requirements is preferred.
• Familiarity with medical terminology and clinical trial procedures.

Responsabilidades

• Assist in screening and recruitment of study participants according to eligibility criteria and protocol.
• Coordinate and schedule participant visits and study-related activities.
• Collect, enter, and verify research data for accuracy and timeliness.
• Conduct participant interviews and support informed consent under supervision.
• Assist with data analysis under supervision of investigators or senior staff.
• Maintain study documentation and regulatory records in compliance with policies and guidelines.
• Support development and translation of study materials and documents.

Conhecimentos

Organisational skills

Attention to detail

Communication skills

Interpersonal skills

Computer literacy

Experience with research databases/EDC

Formação

Bachelor's degree in health-related science

Ferramentas

Electronic Data Capture (EDC) systems

Descrição da vaga

The National University Hospital (NUH) is seeking a Clinical Research Coordinator to support a range of studies from screening and recruitment to data collection and regulatory compliance. You will work with Principal Investigators, clinicians, sponsors, and regulatory bodies to ensure adherence to GCP and institutional policies.

Responsibilities include coordinating participant visits, collecting data, assisting with informed consent, and supporting study materials and dissemination of