Associate Clinical Research Coordinator / Clinical Research Coordinator

KK Women's & Children's Hospital; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A healthcare institution in Singapore is seeking a candidate to provide research support for clinical trials. The role entails assisting Principal Investigators with study initiation, protocol development, and data management while ensuring compliance with regulations. The ideal candidate holds a relevant degree or diploma, has experience in the field, and possesses strong communication and interpersonal skills. Fresh graduates are also welcome to apply, making this position accessible to entry-level professionals.

Qualifications

• Fresh graduate or with at least one year of relevant experience.
• Fresh graduate or minimum one year of relevant experience preferred.
• Proficient in MS Office, with excellent communication skills.

Responsibilities

• Provide research support service for clinical research.
• Assist Principal Investigators with study initiation meetings, IRB submission, and protocol development.
• Support data collection, management, and study monitoring.

Skills

Proficient in using MS Office software

Effectively bilingual

Excellent oral and written communication skill

Excellent interpersonal skill

Excellent interpersonal skill

Education

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

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 support and participate 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