Research Coordinator (DMORT)

The new Research Coordinator will oversee study preparation, data collection, study management and manuscript preparation for studies regarding Integrative Oncology, Breast & Gynaecology, Psycho Oncology and other related projects.

Key Responsibilities

1. Administrative

• Assists the Principal Investigator in submission of accurate and timely closeout documents. Coordinates appropriate and timely payments to participants (if applicable).

1. HBRA/IRB Compliance

• Adherence to the HBRA/IRB by ensuring site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.

1. Risk Mitigation

• Develop the ability to anticipate and mitigate potential risks or non-compliance. Ensure all near-misses and protocol deviations are reported in a timely manner.

1. Patient Recruitment and Follow up

• Select and pre-screen potential patient for study. Taking patient consent in clinic and follow up of the recruited participants.

1. Data Collection

• Maintenance of existing database to input or validate prospective and retrospective data.

Main Requirements:

• Degree in Psychology and/or Health Sciences
• 2 years of related working experience
• Computer literate and able to work on Excel
• Good time-management and communication skills
• Fluent English, able to communicate in Mandarin + other dialects and Malay will be an advantage.
• Team player and strong collaborator
• Meticulous and pleasant demeanour
• Independent, able to work under pressure and effectively multi-task