Clinical Research Coordinator: Impactful Trials

Changi General Hospital Pte Ltd.; Singapore; On-site; SGD 45,000 - 65,000; Full time

Job summary

Changi General Hospital Pte Ltd. is seeking a Clinical Research Coordinator to assist investigators in administering clinical studies, enroll suitable subjects, take vital signs, collect and process biological samples, and enter data.

You will ensure subjects’ safety, perform procedures according to SOPs and ICH-GCP, attend investigator meetings, and liaise with internal and external agencies to support study activities.

Qualifications

• Bachelor’s Degree in Nursing, Science, or another relevant discipline.
• Diploma will be considered for the Associate CRC position.
• Registration with the Singapore Nursing Board is preferred (applicable to State Registered Nurses only)
• At least 2 years’ experience in the coordination of clinical research activities

Responsibilities

• Assist the investigators in overall administration of clinical research activities prior to, during and post study such as enroll suitable subjects, take vital signs, collect and process biological samples, collect and enter data, monitor subjects’ condition
• Work with the study team to ensure subjects’ safety
• Carry out procedures according to the SOP, study protocol and Instruction manual(s) and in compliance with the Regulations and ICH Good Clinical Practice Guideline
• Attend investigator’s meeting (local/overseas) and site initiation meeting as assigned and liaise with relevant internal and external agencies during the course of work

Skills

Clinical trial coordination

Education

Bachelor’s Degree in Nursing, Science, or another relevant discipline

Diploma (Associate CRC position)

Job description

Changi General Hospital Pte Ltd. is seeking a Clinical Research Coordinator to assist investigators in administering clinical studies, enroll suitable subjects, take vital signs, collect and process biological samples, and enter data.

You will ensure subjects’ safety, perform procedures according to SOPs and ICH-GCP, attend investigator meetings, and liaise with internal and external agencies to support study activities.