Research and Clinical Trial Coordinator
UBC The University of British ColumbiaRole Overview
UBC The University of British Columbia is hiring a mid-level Research and Clinical Trial Coordinator. This is a full-time role in CA. Part of UBC The University of British Columbia's Risk hiring, posted last week. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
Staff - Non Union Job Category Non Union Technicians and Research Assistants Job Profile Non Union Salaried - Research Assistant /Technician 3 Job Title Research and Clinical Trial Coordinator Department Lehman Laboratory | Department of Medical Genetics | Faculty of Medicine Compensation Range $4,567.04 - $5,385.67 CAD Monthly Posting End Date June 4, 2026 Note: Applications will be accepted until 11:59 PM on the Posting End Date. This position is subject to the satisfactory completion of required background checks Job End Date June 30, 2027 This position is part-time with 0.5 FTE, equivalent to 18.75 hours per week. Please note that the posted salary range is not prorated to reflect this reduced FTE. 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 The UBC Department of Medical Genetics seeks to be an inspiring and productive community of scholars; an outstanding provider of knowledge, technical expertise, and compassionate care for our patients; contributors to the scientific advance of our discipline; and a credible and respected source of information and advice to society at large. While focusing on areas of genetic medicine that we deem to be particularly important, we view diversity of approach and techniques to be an essential strength of our Department. We acknowledge that the University of British Columbia Faculty of Medicine and its distributed programs, which include four university academic campuses, are located on traditional, ancestral and unceded territories of Indigenous peoples around the province. The Lehman Research Group studies rare genetic disorders, the use of genetic data for risk stratification, and management of inherited metabolic diseases, including clinical trials and registries. This position will be primarily responsible for coordinating small clinical trials conducted by Dr. Lehman and colleagues at the Adult Metabolic Diseases Clinic at Vancouver General Health. The Research and Clinical Trial Coordinator provides administrative, operational, and research support for clinical trials and research studies within the Lehman Research Group in the Department of Medical Genetics. The role is responsible for coordinating clinical trial activities, participant recruitment and consent, regulatory submissions, research documentation, data management, financial tracking, and project communications. The incumbent also supports day-to-day research operations and collaborates with clinical, research, and sponsor teams under the supervision of the Principal Investigator. Organizational Status The Research and Clinical Trial Coordinator will report directly to the Principal Investigator (PI), a medical geneticist and associate professor in the Department of Medical Genetics, and Investigator in the BC Children’s Hospital and Vancouver Coastal Health Research Institutes. The Institutes are affiliated with the University of British Columbia and the Provincial Health Services Authority. Work Performed Coordinates the preparation and submission of research related regulatory documents (ethics, permits, Health Canada submissions, etc.) Coordinates and facilitates patient recruitment, as well as data collection, management, and reporting. Provides project administration with recordkeeping, onboarding, and collaboration with the Clinical Research Unit at VGH. Tracks project communications, maintains research agreements and financial contracts. Assists with the maintenance of supplies and minor research equipment. Assists with lab and program marketing communications, including presentations, newsletters, webpages, and preparing information on research programs for media, fundraising organizations, and potential donors. Assists with the preparation and submission of expense reports for purchases. Tracks and manages project finances, ensuring that expected sponsor payments have been received; invoices have been issued. Coordinates clinical trial tasks and maintains all documentation, including data entry from clinical research forms. Obtains informed consent from participants. Uses clinical trial management software. Liaises with trial sponsors and clinical research organizations, including arranging and hosting medical monitor visits. Performs other duties as required that remain in the appropriate classification. Consequence of Error/Judgement Failure to plan or follow up on initiatives and poor judgment or errors dealing with such matters would have an adverse effect on research participants, reputation, and operational management of the trial. Errors in the oversight of financial accounts and reporting procedures could result in monetary losses and a waste of financial resources or loss of research funding negatively impacting further research initiatives and each collaborating units reputation. Supervision Received The incumbent will receive general supervision from Dr. Anna Lehman. They will receive detailed instructions on assignment of new duties and thereafter receive instructions only on new or unusual problems. They are expected to work collaboratively with all members of the team. Supervision Given The Research and Clinical Trial Coordinator may provide direction to volunteers, students, and new staff in lower classification levels, regarding orientation and research and operational procedures. The incumbent may delegate work as necessary to ensure that the goals of various projects are met in a timely and efficient manner. 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 Experience working on clinical trials is strongly preferred. Experience with processing and interpreting financial statements. Knowledge of UBC and PHSA or VCH admin procedures. Experience with clinical research procedures. Proficiency with Microsoft Office, basic graphic design, and webpage maintenance. Ability to communicate effectively verbally and in writing. Ability to work independently and as part of an interdisciplinary team. Ability to independently prioritize and organize work load. Demonstrated ability to meet deadlines and pay attention to detail. Ability to exercise discretion, tact, and confidentiality. The University of British Columbia is a global centre for research and teaching, consistently ranked among the top 20 public universities globally. A large part of what makes us unique is the community of engaged students, faculty, and staff who are collectively committed to shaping a better world. Recognized as a leading employer in British Columbia and Canada, UBC supports inspired students, faculty and staff on their journey of discovery, and challenges them to realize their greatest potential. New ideas, changing infrastructure, innovative technology, and fresh approaches are opening up possibilities for the future of research, teaching, and work. Are you ready to embrace the future together? Equity and diversity are essential to academic excellence. An open and diverse community fosters the inclusion of voices that have been underrepresented or discouraged. We encourage applications from members of groups that have been marginalized on any grounds enumerated under the B.C. Human Rights Code, including sex, sexual orientation, gender identity or expression, racialization, disability, political belief, religion, marital or family status, age, and/or status as a First Nation, Metis, Inuit, and/or Indigenous person. All qualified candidates are encouraged to apply; however Canadians and permanent residents will be given priority. If you have any accommodation or accessibility needs during the job application process, please contact the Centre for Workplace Accessibility at workplace.accessibility@ubc.ca.
Frequently Asked Questions
How do I apply for the Research and Clinical Trial Coordinator position at UBC The University of British Columbia?
Use the Apply button above to submit your application directly to UBC The University of British Columbia. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Research and Clinical Trial Coordinator position at UBC The University of British Columbia located?
This position is based in CA. UBC The University of British Columbia has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Research and Clinical Trial Coordinator at UBC The University of British Columbia earn?
UBC The University of British Columbia has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Research and Clinical Trial Coordinator role at UBC The University of British Columbia posted?
This role was posted on May 27, 2026 (12 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
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