Clinical Research Coordinator

A motivated Clinical Research Coordinator is sought to join an interventional pain management research team of physicians, imaging technologists, and clinical research specialists. The research coordinator is a health care professional who functions as an administrator, coordinator, educator, and researcher in the organization of investigator initiated and industry sponsored clinical trials. This position is in a community health-based clinic for approximately 12 months (based on length of funding), with the possibility of extension.This position reports to the Research Supervisor.This is a 0.75 FTE, with regular hours Monday to Friday. There will be occasional weekend hours – approximately 1 day per month with advance notice.DUTIES AND RESPONSIBILITIES (include, but are not limited to):Patient Support:· Understand and implement basic research procedures with respect to informed consent, data collection and reporting following ICH-GCP under the guidance and supervision of the Research Supervisor.· Assist in determining eligibility for protocols based on medical history and assessment information in consultation with the Research Team· Collect data for interventional pain management research participants using in-person data collection tools and electronic health record reviews· Implement protocol required activities ensuring excellence in delivery of the research process· Work collaboratively with interventional radiologists, nurses, imaging technologists, operational and administrative staff· Work within the guidelines of privacy and ethical standards· Be comfortable in a diagnostic imaging and interventional pain management settingAdministration:· Have an extensive knowledge of ongoing research projects· Prepare participant research charts including source documentation· Maintaining accurate and detailed records of patient files to ensure they fit all criteria to be enrolled in specific clinical trials· Ensure data entry is accurate and precise and is entered in a timely manner according to research protocolsMonitoring Support:· Preparing and filing study documentation prior to visit· Ensuring the monitor has everything required for the visit under the guidance of the Research Supervisor· Constant communication with monitor and coordinator to ensure an effective visit· Obtaining proper documentation before during and after visit, as required· Facilitate regulatory document completion and updates as necessary· Ongoing maintenance of study binders· Ensure all required documentation is available and filed properlyCommunication/Relationships:· Work collaboratively with the Research Team· Develop and maintain communication with various stakeholdersQUALIFICATIONS/REQUIREMENTS:· Undergraduate degree in life sciences and/or clinical research experience· Minimum two years’ experience in a clinical research position· Specialized certification - TCPS 2 and ICH-GCP certification· SoCRA or ACRP certification an asset, but not required· Organized and efficient individual with strong attention to detail· Experience entering data in EDC formats is an asset, but not required· Intermediate to advanced skills in Microsoft Office Suite (Word, Outlook, Excel, PowerPoint), Internet skills· Demonstrated ability to work independently and as part of a teamSALARY/BENEFITS:· Compensation to be commensurate with experiencePlease apply with Cover Letter and CV to research@beamradiology.comApplication Deadline: November 25, 2025We would like to thank all applicants in advance for submitting their resumes. Please note, only those candidates chosen to continue on through the selection process will be contacted.