Clinical Research Coordinator - Up $
Subject recruitment, scheduling, and data entry.
Obtain consent, administer study questionnaires, and follow up with study participants.
Work closely with the research team, clinicians, clinic staff, and other internal departments to ensure research study needs are met.
Work on tight timelines, set sensible targets, and achieve research deliverables.
Conduct research study activities such as patient recruitment, data collection, and data management.
Assist in data collection from electronic health records.
Set up and maintain study investigator files, including records of consent and blood collection.
Maintain study records in databases such as REDCap and electronic health record systems.
Ensure strict adherence to research protocols.
Liaise with investigators, clinicians, and laboratory teams to set up clinical workflows for research recruitment at multiple departments.
Prepare documentation for audit purposes.
Coordinate the submission of new IRB applications, study amendments, and annual reports.
Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements, and local regulations.
Assist with other similar duties delegated by the Principal Investigator.
Requirements
Bachelor's degree in Science, Public Health, or Social Science.
Proficiency in Microsoft Office applications.
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Clinical Coordinator • Queenstown, New Zealand