Clinical Research Coordinator (Respiratory & Critical Care Medicine) (Contract)

Singapore General Hospital; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading health institution in Singapore is seeking a candidate to provide research support services for Respiratory & CCM clinical research. The role involves patient recruitment, data collection, and collaboration with investigators in clinical trials. A Bachelor in a relevant field and strong knowledge of computer applications are required. This position offers an opportunity to work closely with clinical teams and contribute to innovative research.

Qualifications

• Good knowledge of computer applications.
• Team-oriented with strong coordination and organisational skills.
• Certificate in Basic Good Clinical Practice (GCP) is advantageous.

Responsibilities

• Assist in screening of patients for recruitment.
• Enroll patients into the clinical study.
• Organize patients’ visits and carry out required procedures.
• Collect data and complete clinical reports.
• Record and report adverse events.
• Maintain organization of site file.
• Assist investigators in conducting clinical trials per guidelines.
• Communicate closely with sponsor company and investigators.

Skills

Knowledge of computer applications

Team-oriented

Strong coordination and organisational skills

Education

Bachelor in Science, Health Science, Nursing or a related field

Tools

Microsoft Access

Excel

PowerPoint

SPSS

Job description

The incumbent will provide research support service for Respiratory & CCM clinical research. He/she works closely with the Principal Investigator (PI) and members of the Respiratory & CCM team.

Responsibilities

• To assist in screening of patients for recruitment

• To assist in enrolling patients into the clinical study

• To organize patients’ visits, and ensure that all the required procedures are carried out

• To collect data and complete clinical reports

• To record and report adverse events

• To assist in maintaining and organization of site file

• To assist the investigators in conducting clinical trial according to Good Clinical Practice guidelines.

• To communicate closely with the sponsor company and the investigators and provide ancillary services for the clinical trials.

• Other duties as specified by Department Head or Supervisor.

Qualifications

• Bachelor in Science, Health Science, Nursing or a related field

• Good knowledge of computer applications e.g. Microsoft Access and Excel, PowerPoint, SPSS

• Team-oriented with strong coordination and organisational skills

• Candidate with certificate in Basic Good Clinical Practice (GCP) or registered nurse with SNB would be an advantage