The Role of a Clinical Research Coordinator
* This is an exciting opportunity to support a clinical research study and maintain a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.
Responsibilities:
* Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
* Supporting screening and enrolment of patients and collection of related documents
* Planning and coordinating logistical activity for study procedures according to the study protocol
* Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
* Management and shipment of biological samples
* Performing ECG, taking vital signs, phlebotomy
* Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
* Administrative research tasks
Requirements:
* BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
* Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
* Basic knowledge of medical terminology
* Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
* Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
* Good organizational skills with the ability to pay close attention to detail