Note: Applications will be accepted until 11:59 PM on the Posting End Date.
Job End Date
May 13, 2026This 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.
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
This individual is a member of the Vaccine Evaluation Center (VEC) whose primary role is to perform research activities related to data handling and conducts a wide range of tasks related to data management and storage.
Organizational Status
Interfaces with Data Coordinators, Study Coordinators, and Senior Data Manager.
Interfaces with other clinical research sites disseminating data queries and facilitating quality assurance regarding data collected.
Work Performed
Provides quality control monitoring for data collection following and interpreting GCP guidelines, ensuring accuracy, completeness, legibility, and verifiability of source information.
Tests new data entry databases for ease of use within the data management area.
Writes user manuals for data entry staff.
Documents the structure of the already developed database.
Documents the data management process for each study.
Perfoms logical checks of the data, queries and edits the data when errors are found
Prepares the database for the statistical team's use and prepares the computerized data for long-term storage according to VEC policies.
Downloading and organizing relevant study data as requested by supervisors and in alignment with study protocols.
Assisting in the development of research study databases and database user manuals.
Consequence of Error/Judgement
Duties are performed according to operating procedures and VEC policies. Decisions are made for the tasks at hand as related to the jo. Some non-routine decisions are made without consultation.
Consequences of errors in decision making may affect the integrity of databases and/or integrity of study outcomes. As a result, the reputation of the VEC may be jeopardized.
Supervision Received
The individual is expected to know the standard tasks that need to be done for the project and carry them out independently, reporting progress to their coordinator. Supervision in limited in that tasks are assigned and the end result is reviewed. Supervision comes from the data coordinators.
Supervision Given
Provides technical guidance to other project team members and is expected to provide training to other research assistants.
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
- Undergraduate degree in computer science with additional courses in the health care field
- Experience in vaccine clinical trials
- Experience using SAS Analytics Software and R programming
- Ability to communicate effectively verbally and in writing
- Ability to maintain accuracy and attention to detail
- Ability to work effectively independently and in a team environment
- Have excellent organizational skills as they are required to work on more than one study at a time.
- Experience in database management
- A sound understanding of vaccines and their appropriate use
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Are you passionate about data management and research? The Vaccine Evaluation Centre (VEC) at UBC Off-Campus Hospital Sites is on the lookout for a dedicated Data Research Assistant (VEC) to join our vibrant team! In this role, you will be immersed in a supportive environment where your contributions will directly impact vaccine research. You'll be primarily engaged in managing and handling vital research data, ensuring that the information is accurate, complete, and verifiable according to Good Clinical Practice (GCP) guidelines. No two days will be the same as you will interface with Data Coordinators, Study Coordinators, and the Senior Data Manager. Your responsibilities will include conducting quality control monitoring, writing user manuals for data entry staff, and preparing data for long-term storage. You’ll be the go-to person for testing new data entry databases and providing technical guidance to team members. The position requires strong attention to detail and the ability to work independently, while also thriving in a collaborative team environment. If you have a relevant technical background or a university degree in a related discipline, along with at least three years of experience, we would love to hear from you. Experience in vaccine clinical trials and proficiency in SAS Analytics Software and R programming are definitely an asset. Join us in our mission to conduct world-class research while fostering equity, diversity, and inclusion in the workplace!
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