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Data Coordinator and Developer (VEC)

The University of British Columbia
Vancouver, CAN
Full-time
Entry
Onsite
CAD 6,631.67 to CAD 9,533.25 per month
Discovered 1 weeks ago
Clinical data managementClinical trialsVaccine trialsData coordinationData management systemsDatabase design and maintenance
Free

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Role Overview

The Data Coordinator and Developer supports the Vaccine Evaluation Centre within UBC's Department of Paediatrics.

The role consults with investigators on data identification, collection processes, and study outcomes across multiple studies.

The position coordinates and supervises data-team work and may provide project management support.

Compensation

  • The compensation range is CAD 6,631.67 to CAD 9,533.25 per month.
  • The job end date is September 1, 2027.

Program Coordination

  • Oversee nurse-monitor tasks at 14 IMPACT Centers for surveillance and externally funded projects.
  • Prepare budgets, statements of work, protocols, and task authorization requests.
  • Monitor contract deliverables and data deliverables across IMPACT Centers.
  • Complete the annual Systems Overview and Data Product Inventory for the Public Health Agency of Canada.
  • Organize annual meetings and support the Executive Committee and IMPACT data working groups.
  • Maintain directories, reporting pathways, tracking schedules, coding lists, orientation materials, and training materials.

Data Management and Development

  • Develop specialized case report forms and user manuals for individual studies.
  • Design and implement systems that manage data from field collection through analysis and long-term storage.
  • Maintain study databases until data-cleaning requirements are complete and databases are transferred to the statistician.
  • Customize, maintain, and upgrade routine and complex databases.
  • Work with statisticians on descriptive aggregate statistics and data-management decisions.
  • Provide basic statistical programming support when required by an analysis plan.

Supervision and Communication

  • Follow up with study centers regarding questions, concerns, workloads, and priorities.
  • Coordinate internal management and working groups and communicate with the National Microbiology Laboratory about shipments.
  • Train and orient new study monitors and report under-performing sites or monitors to the Executive Committee.
  • Assign, monitor, and evaluate data-staff work and adjust schedules as priorities change.

Minimum Qualifications

  • An undergraduate degree in a relevant discipline is required.
  • At least two years of related experience, or an equivalent combination of education and experience, is required.
  • Clinical-trial data-management experience is required, with vaccine-trial experience preferred.
  • At least two years of supervisory experience is preferred.
  • Knowledge of web-based clinical data management software, SAS, advanced programming, and information management is required.
  • Effective communication, analytical, decision-making, problem-solving, accuracy, and prioritization skills are required.

Workplace and Reporting

  • The position reports to the Senior Data Manager and study investigators.
  • For IMPACT program responsibilities, the role also reports to the IMPACT Executive Committee.
  • The source does not specify whether the position is onsite, hybrid, remote, or field-based.

Application Notes

  • Applications are accepted until 11:59 PM on September 11, 2026.
  • The position is expected to be filled by promotion or reassignment and is posted to inform employees of the vacancy.
  • Satisfactory completion of required background checks is required.

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