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 setting
Administration:
- 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 protocols
Monitoring 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 properly
Communication/Relationships:
- Work collaboratively with the Research Team
- Develop and maintain communication with various stakeholders
QUALIFICATIONS/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 team
SALARY/BENEFITS:
- Compensation to be commensurate with experience
Please apply with Cover Letter and CV to [email protected]
We 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.
Job Types: Full-time, Part-time
Pay: From $23.40 per hour
Benefits:
- Casual dress
- Company events
- Dental care
- Disability insurance
- Employee assistance program
- Extended health care
- Life insurance
- On-site parking
- Paid time off
- Vision care
Work Location: Hybrid remote in Calgary, AB
