Clinical Research Associate
3 weeks ago
Staff - Non Union
Job Category
Non Union Technicians and Research Assistants
Job Profile
Non Union Salaried - Research Assistant /Technician 3
Job Title
Clinical Research Associate (CRA)
Department
Michael Cuccione Childhood Cancer Research Program | Department of Paediatrics
Compensation Range
$4,434.02 - $5,228.81 CAD Monthly
Posting End Date
April 20, 2024
**Note**: Applications will be accepted until 11:59 PM on the day prior to the Posting End Date above.
Job End Date
Apr 17, 2025
This position is expected to be filled by promotion/reassignment and is included here to inform you of its vacancy at the University.
This offer is conditional upon successful completion of a Criminal Record Check.
**Note**: Only the Full Time Compensation Range is displayed on the job posting details advertised on the UBC Career sites.
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.
WORK PERFORMED
To coordinate clinical research protocols, including but not limited to Phases I, II and III chemotherapy studies, hematology studies, bone marrow transplant studies, supportive care studies and ancillary studies:
Ensuring adherence to and maintenance of protocols
Maintaining protocols and associated documents to ensure they are up-to date
Responsible for the day-to-day operation of multi-site investigator initiated project
Coordinating and liaising closely with the interdisciplinary staff, study sponsors and consortiums identifying and screening potential study participants
Preparing source documentation for review and confirmation of eligibility criteria
Overseeing registration process of patients on clinical studies
Creation of novel study specific documents and work flows
Responsible for collecting documentation, organization and accurate and timely completion and submission of paper and electronic data capture forms
Reporting adverse drug reactions in consultation with physician and in accordance with protocol-specific guidelines
Procuring and safely shipping as well as maintaining accurate documentation of study specimens from various sources according to protocol guidelines and federal regulations
Acting as liaison with health care team and laboratory team, both on-site and outside the institution, for project management and information exchange regarding clinical studies
Performing data entry and managing research databases with accuracy
Preparing and participating in audits and study monitoring visits from various regulatory bodies
Attending conferences and meetings, possibly involving travel
Timely completion of required regulatory certificates and tutorials
Maintaining clinical research education and regulatory certifications
Providing back-up for other team members while sick or on holidays
If not already obtained, the division will support training for clinical research professional certification through the Society of Clinical Research Associates
Performing other related tasks and projects as deemed necessary
CONSEQUENCE OF ERROR
Consequences of error are high and this is a position with significant responsibility. The data submitted impacts the direction of future studies. Errors could impact upon the reputation of the program as a whole and jeopardize the options for collaborative participation with industry, government and other centers.
SUPERVISION RECEIVED
It is expected that the RT3 will demonstrate the ability to work independently once training has been successfully completed. The RT3 will be required to problem solve on a limited basis.
SUPERVISION GIVEN
The RT 3 will receive supervision and direction from the RT 4's or M&P within the Program.
MINIMUM QUALIFICATIONS
Completion of a relevant technical program or a university degree in a relevant discipline and a minimum three years of related experience or an equivalent combination of education and experience.
Willingness to respect diverse perspectives, including perspectives in conflict with one's own.
Demonstrates a commitment to enhancing one's own awareness, knowledge, and skills related to equity, diversity, and inclusion.
PREFERRED QUALIFICATIONS
Clinical research professional certification through the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP), transportation of Dangerous Goods Certificate preferred.
**Assets**: Demonstrated knowledge and experience with Pediatric oncology, familiarity with database management programs. Knowledge of Good Clinical Practice. Attentive to detail, with the ability to work quickly and accurately. Medium to high degree of computer literacy including familiarity with Microsoft Word, Access and Exce
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