Co-Ordinator
Roles and Responsibilities
- Manage research datasets. This includes extraction of data from medical records, data cleaning and preparation, data entry, data harmonisation and analysis of trends
- Build reports and dashboards for data visualisation
- Ensure that all data work comply with existing data ethics and legal requirements
- 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:
- Recruit patients in the clinic and assist in screening, recruitment and consent taking of participants;
- Tissue banking and blood processing activities;
- Liaise with relevant internal and external agencies during the course of work;
- Ensure timely submission of progress report to the relevant agencies and authorities and renewal of ECOS approvals;
- Undertake any other tasks assigned by the Supervisor.
Requirements
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Diploma or Degree in Biomedical Sciences or equivalent;
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Working experience in academic or clinical research would be advantageous;
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A strong interest in data management;
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Proficient in English and Mandarin. Proficiency in Malay and Tamil will be an added advantage. We are seeking candidates proficient in Mandarin/Malay/Tamil to effectively communicate with Mandarin/Malay/Tamil-speaking clients.
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Proficient in MS Word, MS Excel, Power Point and Outlook;
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Knowledge in research ethics and preferably completed the CITI;
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Good written and oral communication skills;
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Team-oriented with strong coordination and organisational skills;
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Able to work independently and comfortable to multi-task / handle a few projects concurrently