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 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
