Clinical Research Coordinator, Surgery - Saskatoon, Canada - University of Saskatchewan
Description
Clinical Research Coordinator, Surgery:
Primary Purpose:
Currently, our neurosurgery spine research team is looking for a Clinical Research Coordinator who can work for us, supporting several spine-related research projects.
The Research Coordinator will work closely with the sponsors, clinicians and other team members to conduct the research projects, the research coordinator will be responsible for assisting in the planning, managing, and coordination of clinical research activities.
Nature of Work:
Describe the reporting structure, physical environment, judgment/discretion required; level of decision making, pace of work/work cycles and what to expect in the position.
Note if travel or shift work is required.
The Research coordinator will be responsible for the overall coordination for the spine research projects at Neurosurgery, College of Medicine, and University of Saskatchewan.
This will involve working with local, national and international research partners, which includes both spine registries and industry partners working on spinal cord injury clinical trials.
Interest in working with spine research participants and families, occasional weekend/ evening/holidays work may be required because of conducting acute clinical trials.
Typical Duties or Accountabilities:
List the typical duties or accountabilities. Accountabilities support the overall direction of the unit by defining what outcomes are expected over the longer term. Accountabilites need to be supplemented by annual measurable goals.
To conduct the clinical research projects and clinical trial according to the study protocol, Good Clinical Practice (GCP), the Standard Operating Procedures
(SOP), following the guidelines and privacy legislation
:
The preparation of submissions to Research Ethics Boards, manage the process for research agreement and budget, preparation of annual report and financial report.
To recruit and screen patients for participation in clinical research studies, complete documentation and data entry.
To obtain proper written informed consent from each study participant prior to participation in the study, coordinating clinical research visits, participant follow-up communications.
To obtain vital signs as required per protocol (i.e. blood pressure, temperature, heart rate, weight & height). To monitor and report all adverse experiences and abnormal results to the Investigator and Sponsor. Competence in blood handling and processing of blood samples, certificate of training transportation of dangerous goods is required.Education:
minimum Bachelor's Degree in health related field, medicine, nurse or equivalent.
Experience:
At minimum, 2 year experience in clinical research and conducting clinical trials.
Skills:
Directly related to the position's accountabilities and nature of work. This section generally includes statements that reflect effective interpersonal, communication, and organizational skills. Job specific skills should also be included.
Knowledge of general clinical research procedures and regulatory requirements. Experience collecting complicated clinical research data.
Proficiency with computer skills and standard software (MS Office, SharePoint, etc), knowledge of internet, clinical research database and medical electronic database.
Department:
Surgery
Status:
Term 12 months with the possibility of extension
Employment Group:
Research Positions - Non-union
Full Time Equivalent (FTE):
1.0
Salary:
The salary range, based on 1.0 FTE, is $ per hour. The starting salary will be commensurate with education and experience.
Salary Phase/Band:
Salary Band 7
Posted Date:
2/13/2024
Closing Date:
3/26/2024
Number of Openings:
1
Work Location:
On Campus
Criminal Record Check:
Not Applicable
Driver's License and Abstract Check:
Not Applicable
Education/Credential Verification:
Not Applicable
Vulnerable Sector Check:
Not Applicable
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