MOSAIC Research Coordinator

Socket.dev; Vancouver; Hybrid; CAD 54,000 - 64,000; Full time

Job summary

University of British Columbia’s Division of Cardiology in the Department of Medicine invites applications for a MOSAIC Research Coordinator to support a provincial study on echocardiography, genomics and AI. The role will coordinate all aspects of the MOSAIC project, ensuring timely, compliant execution while fostering collaboration among researchers and hospital staff across BC and Yukon.

Primarily on-site with potential for up to one remote workday per week, the successful candidate will work

Qualifications

• Completion of a relevant technical program or a university degree and a minimum three years of related experience.
• Demonstrates commitment to equity, diversity, and inclusion.

Responsibilities

• Recruit and enroll study participants, including informed consent and scheduling visits.
• Coordinate daily study operations, monitor recruitment progress and participant retention metrics.
• Maintain meticulous documentation and ensure adherence to study protocols.
• Assist with start-up and maintenance of study sites, including REB applications and amendments.
• Educate participants on protocol requirements and data collection tools.
• Monitor subjects for outcomes and report as specified in the protocol.
• Participate in research team meetings and communicate updates to the research manager.
• Ensure compliance with Good Clinical Practice (GCP) and regulatory standards.
• Develop and update SOPs to align with sponsor requirements.
• Access study data from hospital EHRs and PACS systems.
• Manage participant data using REDCap or similar tools.
• Coordinate data and sample collection, storage, and shipment per protocols.
• Assist in developing research proposals and grant applications.
• Conduct literature reviews and summarize findings.
• Travel between hospital sites to support study operations.

Skills

Interpersonal communication

Data management

Time management

Attention to detail

Research coordination

Education

University degree

Relevant technical program

Tools

REDCap

EDC

Word

Excel

PowerPoint

Job description

Staff - Non Union

Job Category

Non Union Technicians and Research Assistants

Job Profile

Non Union Salaried - Research Assistant /Technician 3

Job Title

MOSAIC Research Coordinator

Department

Tsang Laboratory Division of Cardiology | Department of Medicine | Faculty of Medicine

Compensation Range

$4,845.17 - $5,713.66 CAD Monthly

Posting End Date

August 30, 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

September 13, 2027

Please note, this role is primarily based on-site, and may be eligible for up to one remote workday per week, subject to operational requirements. The successful candidate will be required to work across four hospital sites in Vancouver: Vancouver General Hospital, St. Paul's Hospital, Mount Saint Joseph Hospital, and UBC Hospital.

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 Division of Cardiology in the Department of Medicine at the University of British Columbia is seeking a highly motivated and detail-oriented Research Coordinator to support a provincial study on echocardiography, genomics and AI. The Multi-Omics and Sonography to Advance Integrated Cardiac Care (MOSAIC) study is aimed at improving cardiovascular disease risk prediction and care pathways across diverse populations in British Columbia (BC) and Yukon to advance personalized health innovations. The Research Coordinator will play a critical role in coordinating all aspects of the research study, ensuring timely, efficient, and compliant execution of study-related tasks while fostering a collaborative research environment. This role requires exceptional organizational and interpersonal communication skills, a strong ability to manage competing priorities, and a commitment to ethical research practices.

Please note, this role is primarily based on‑site, and may be eligible for up to one remote workday per week, subject to operational requirements. The successful candidate will be required to work across four hospital sites in Vancouver: Vancouver General Hospital, St. Paul's Hospital, Mount Saint Joseph Hospital, and UBC Hospital.

Organizational Status

The Research Coordinator will report to the Principal Investigators while working closely with research staff, clinical teams, and external stakeholders. This position requires frequent interaction with study participants, hospital staff, sponsors, and regulatory bodies.

Work Performed

• Responsible for recruiting and enrolling study participants, including obtaining informed consent, scheduling laboratory visits, and coordinating participant follow‑up activities.
• Coordinates daily study operations, including monitoring recruitment progress and participant retention metrics, and identifying and implementing strategies to enhance enrollment, participant engagement and operational efficiency. Liaise with physicians and other hospital staff to establish and coordinate study operations within several departments, including laboratories and outpatient services.
• Maintain meticulous documentation and ensure strict adherence to study protocols.
• Assist the research managers with the start‑up and maintenance of multiple research study sites, including obtaining operational approvals and Research Ethics Board (REB) applications, amendments, and renewals
• Educate study participants on protocol requirements, schedules, and data collection tools.
• Monitors study subjects for outcome events appropriately and report as specified in study protocol.
• Actively participate in research team meetings. Provide regular updates on research activities, establish effective communication with all team members, and ensure timely notification of adverse events and other issues to the research manager
• Ensure compliance with Good Clinical Practice (GCP) guidelines and all institutional, national, and international regulations.
• Develop and update Standard Operating Procedures (SOPs) to align with sponsor requirements.
• Access study data from various sources, including hospital electronic health records and picture archiving and communication systems.
• Manage participant data using tools such as REDCap, ensuring data accuracy and integrity.
• Coordinate data and sample collection, storage, and shipment of biological specimens according to study protocols.
• Assist in developing research proposals, grant applications and study source documents.
• Conduct literature review and summarize findings.
• May contribute to academic publications and present at academic conferences; and
• Travels between hospital sites as required to support study operations and research activities.
• Perform other duties as needed.

Consequence of Error/Judgement

Failure to perform duties ethically or accurately could compromise study outcomes, jeopardize participant safety, and impact the credibility of the research program. Strict confidentiality and adherence to ethical standards are essential.

Supervision Received

Works under the supervision of principal investigators and research managers.

Supervision Given

The research coordinator may train volunteers, students and staff in research and projects.

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

• Exceptional interpersonal communication skills and experience in a patient‑facing or customer service role
• Recent experience in a clinical research setting.
• Proficiency with database systems (e.g., REDCap, EDC) and standard office tools (Word, Excel, PowerPoint).
• Strong time management skills with the ability to prioritize competing tasks and responsibilities. Demonstrated expertise in patient interaction, participant recruitment and participant retention
• Strong analytical and organizational skills, with the ability to assist with multiple projects and meet strict deadlines.
• Certification in Good Clinical Practice (GCP) or clinical trial management is preferred.
• Knowledge of Indigenous‑specific anti‑racism and cultural safety is an asset.
• Proven ability to prepare and submit online Research Ethics Board (REB) applications, amendments, and renewals with a strong understanding of regulatory requirements and ethical standards.
• Solid judgment and discretion in maintaining confidentiality and handling sensitive information.
• Exceptional attention to detail and accuracy in documentation, data entry, and reporting.
• Demonstrate the ability to collaborate with diverse teams and communicate effectively with investigators, participants, and other stakeholders.
• Ability to work independently with minimal supervision and contribute to a dynamic, fast‑paced research environment.
• Familiarity with specimen collection, handling, storage, and shipment processes in clinical research. Biosafety for Study Team Members certificate and Transportation of Dangerous Goods certificate considered an asset
• Knowledge of advanced data management systems or clinical trial management systems (CTMS).