Job Purpose

The Clinical Research Coordinator is responsible for assisting principal clinical investigators with prospective and retrospective data collection and entering data into databases for patients with haematologic malignancies and those undergoing stem cell transplantation and cellular therapy, data collection for patients enrolled into research studies, database maintenance of research studies, data provision for conference presentations and maintain study status updates by submission of documents and/or data to DSRB and registries.

Primary Responsibilities and Duties (80%)

1. Collecting clinical data by accessing patient’s medical records to extract information on current and past medical history, medications, laboratory, imaging results.
2. Provide clinical support such as data entry and transcription of information on excel dataset, electronic CRFs and Redcap Master database.