Co-Ordinator

Roles and Responsibilities

1. Manage research datasets. This includes extraction of data from medical records, data cleaning and preparation, data entry, data harmonisation and analysis of trends
2. Build reports and dashboards for data visualisation
3. Ensure that all data work comply with existing data ethics and legal requirements
4. Assist and support Principal Investigators (PI) in their clinical research activities (starting from study start-up till study end including study closure activities) such as:
5. Recruit patients in the clinic and assist in screening, recruitment and consent taking of participants;
6. Tissue banking and blood processing activities;
7. Liaise with relevant internal and external agencies during the course of work;
8. Ensure timely submission of progress report to the relevant agencies and authorities and renewal of ECOS approvals;
9. Undertake any other tasks assigned by the Supervisor.

Requirements

1. Diploma or Degree in Biomedical Sciences or equivalent;
2. Working experience in academic or clinical research would be advantageous;
3. A strong interest in data management;
4. Proficient in English and Mandarin. Proficiency in Malay and Tamil will be an added advantage.
5. Proficient in MS Word, MS Excel, Power Point and Outlook;
6. Knowledge in research ethics and preferably completed the CITI;
7. Good written and oral communication skills;
8. Team-oriented with strong coordination and organisational skills;
9. Able to work independently and comfortable to multi-task / handle a few projects concurrently