Research Coordinator

Staff - Non Union### ##
** Job Category
** M&P - AAPS##
** Job Profile
** AAPS Salaried - Research and Facilitation, Level A### ##
** Job Title
** Research Coordinator### ##
** Department
* * Hsiung Laboratory Division of Neurology | Department of Medicine | Faculty of Medicine### ##
** Compensation Range**$5,365.42 - $7,709.92 CAD Monthly The Compensation Range is the span between the minimum and maximum base salary for a position. The midpoint of the range is approximately halfway between the minimum and the maximum and represents an employee that possesses full job knowledge, qualifications and experience for the position. In the normal course, employees will be hired, transferred or promoted between the minimum and midpoint of the salary range for a job.###

##
** Posting End Date
** January 9, 2026
*
* Note:

** Applications will be accepted until 11:59 PM on the Posting End Date.
** Job End Date
** January 31, 2027

At UBC, we believe that attracting and sustaining a diverse workforce is key to the successful pursuit of excellence in research, innovation, and learning for all faculty, staff and students.

Our commitment to employment equity helps achieve inclusion and fairness, brings rich diversity to UBC as a workplace, and creates the necessary conditions for a rewarding career.
** Job Summary
** To coordinate clinical and laboratory research studies in dementia including the "Asian Cohort for Alzheimer Disease" (ACAD) study, and to assist in the development and conduction of other clinical trials in Alzheimer and Related Disorders. The office is on the second floor of the Koerner Pavilion in the UBC Hospital, or on the second floor of the  Centre for Brain Health, with both natural and fluorescent lighting.

There are no known hazards.

** Organizational Status
** Reports directly to the Principal Investigator and works with the other PIs of the research unit. Interacts and works closely and collaboratively with all the staff members of the Clinic for Alzheimer Disease and Related Disorders to coordinate research studies and other future research studies in this unit. Able to independently implement all study protocols in compliance with regulatory and ethical standards.

Provides liaison and operational oversight and coordinate with the other research sites (such as the leading site at the University of Pennsylvania (U of Penn)). Maintain contact with other collaborating organizations and the study team
** Work Performed
*** Implements all study procedures in accordance with research protocols
* Screens and recruits research subjects and devises strategies for effective recruitment
* Liaise with other potential referral sources (i.e. Alzheimer Society of BC, other family doctor offices, and specialist offices) to obtain the required number of participants in the study
* Coordinate the ACAD study research visits at UBC Centre for Brain Health with oversight by the U of Penn site
* Provides patient education on study background, purpose, procedures and potential benefits and risks, in order to obtain proper informed consents for subject participations in studies
* Manage research budget for ACAD and ensure it is compliant with the study protocol
* Conducts patient clinical, behavioral and neuropsychological assessments and coordinates the operations of the trial
* Coordinates hospital service and fee approval for research studies
* Prepares and updates submissions to the University Clinical Research Ethics Board (CREB)
* Writes and prepares regulatory documents
* Ensures accurate and timely data collection and troubleshoots data collection issues
* Liaises with the Data Management Core at the Centre for Health Outcomes and Evaluation Sciences (CHEOS)
* Organizes collection, storage and shipment of biological samples
* Will coordinate forthcoming research grant submissions for further clinical trials
** Consequence of Error/Judgement
*** Study data and integrity may be jeopardized if not conducted according to ethical requirements as laid out by the University and other regulatory authorities and if the project management is not successful
* Patient confidentiality can be compromised if files and information are not kept secure.
* An error within the realm of a research study may result in biased or incomplete data and skewed study results
* Any procedure or data record as part of the project must be accurate and must accurately reflect the work performed
* An error in scheduling study subject visits may result in a protocol deviation and or significantly increase study expenditures
* An error in the collection, storage or shipment of biological samples could result in them being rendered ineffective, requiring repeat collection, increasing participant burden, and increasing expense
** Supervision Received
** Reports directly to the Principal Investigators. The Principal Investigators will oversee performance and results of the study.

** Supervision Given
** May need to supervise work study students when they are available.

** Minimum…