Associate Clinical Research Coordinator / Clinical Research Coordinator

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

Job summary

Singapore General Hospital is seeking a candidate to provide research support for clinical studies in line with regulatory and GCP standards. You will work with Principal Investigators to organise initiation meetings, assist with IRB submissions and protocol development, and handle recruitment, data collection and study documentation.

The role also involves coordinating study logistics, monitoring activities, and contributing to the hospital’s mission of delivering quality patient care,

Qualifications

• Bachelor degree in Nursing/Science or diploma in Clinical Trials Management.
• Fresh graduate or with at least one year of relevant experience.
• Proficient in MS Office software.
• Effectively bilingual.
• Excellent oral and written communication skill.
• Excellent interpersonal skill.

Responsibilities

• Provide research support for clinical research per regulatory, GCP and protocol requirements.
• Coordinate organisation of study initiation meetings and IRB submissions.
• Assist with protocol development, study logistics, recruitment, data collection and document management.
• Support study monitoring and other duties as assigned.
• Contribute to SGH mission of providing quality patient care, education and research.

Skills

Bilingual

Oral and written communication

Interpersonal skills

Team collaboration

Education

Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management

Tools

MS Office

Job description

Job Description

You will provide research support service for clinical research, in accordance to the applicable regulatory, Good Clinical Practice and protocol requirements. You will work closely with the Principal Investigators (PIs), to assist them with organisation of study initiation meetings, IRB submission, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.

You will provide research support service for clinical research, in accordance to the applicable regulatory, Good Clinical Practice and protocol requirements. You will work closely with the Principal Investigators (PIs), to assist them with organisation of study initiation meetings, IRB submission, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.

You will support and participates in the SGH mission of providing quality patient care, education, research.

Job Requirements

• Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management
• Fresh graduate or with at least one year of relevant experience
• Proficient in using MS Office software
• Effectively bilingual.
• Excellent oral and written communication skill
• Excellent interpersonal skill