Clinical Research Nurse

The University of British Columbia; Vancouver; On-site; CAD 74,000 - 106,000; Full time

Job summary

The University of British Columbia seeks a Clinical Research Nurse to support the Division of Cardiology research programs within the Department of Medicine. You will coordinate high-quality cardiac studies, recruit and consent participants, and ensure regulatory and clinical standards are met across multi-centre collaborations with academic and industry partners.

You will oversee study documentation, participate in budget planning, and contribute to data collection and safety reporting,

Qualifications

• Registered nurse with clinical trial experience.
• Familiar with GCP and regulatory submissions.
• Experience coordinating cardiovascular research studies.

Responsibilities

• Develops and supervises implementation of clinical trials.
• Coordinates data and specimen transfer and oversees documentation.
• Prepares regulatory and ethical submissions and hospital approvals.
• Engages with investigators, sponsors and multidisciplinary teams.
• Ensures subject safety, protocol adherence, and timely reporting.
• Oversees study budgets and funding applications.

Skills

Nursing

Clinical Research

GCP

Patient Recruitment

Data Collection

Regulatory Compliance

Job description

Job Title

Clinical Research Nurse

Job Category

M&P - AAPS

Job Profile

AAPS Salaried - Nursing, Level A

Job Family Group

Staff - Non Union

Department

VGH Research Group Support Division of Cardiology | Department of Medicine | Faculty of Medicine

Compensation Range

$6,631.67 - $9,533.25 CAD Monthly The Compensation Range is the span between the minimum and maximum base salary for a position. The midpoint of the range is approximately halfway between the minimum and the maximum and represents an employee that possesses full job knowledge, qualifications and experience for the position. In the normal course, employees will be hired, transferred or promoted between the minimum and midpoint of the salary range for a job.

Job End Date

October 18, 2027

Posting End Date

November 29, 2026 Note: Applications will be accepted until 11:59 PM on the Posting End Date.

Employment Equity Statement

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 Clinical Research Nurse supports clinical research activities for the Division of Cardiology in the Department of Medicine, coordinating and delivering high-quality cardiac research studies in accordance with regulatory, ethical, and clinical standards. The role involves patient recruitment and consent, study coordination, and data collection, while working closely with investigators, multidisciplinary clinical teams, and academic and industry research partners. The Clinical Research Nurse ensures participant safety, protocol adherence, and accurate documentation, and contributes to the advancement of evidence-based cardiovascular care.

Organizational Status

This position works under the supervision of Principal Investigators within the Division of Cardiology and Research Manager. Collaborates with researchers, coordinators, and hospital staff to ensure that study-related tasks are completed.

Work Performed

• Develops and supervises implementation of clinical trials.
• Develops and promotes activities relating to research and multi-centre clinical trials locally and internationally.
• Designs and develops data collection methodologies, instruments and databases.
• Oversees and coordinates data and specimen transfer.
• Conducts preliminary data analysis on study data bases.
• Generates progress and interim reports for presentation.
• Prepares and follows up on initiatives or issues relating to research and clinical trials.
• A key liaison with research manager, Principal Investigator (PI) and sponsors.
• Provides leadership in all areas of research and clinical trials in the hospital and community.
• Participates in developing and evaluating strategies to meet the clinical trial goals and objectives.
• Reviews and implements research protocol.
• Preparation of study documents including ethical submissions, regulatory documents and hospital research approvals.
• Assists in clinical trial budgets.
• Participates in identifying and applying for additional funding.
• Facilitates participation of medical students and physicians in training.
• Teaches and provides leadership to staff in associated areas within the hospital regarding the study purpose, goals, objectives and requirements.
• Independently evaluates eligible patients for study entry.
• Obtains and documents patient informed consent as per GCP(Good Clinical Practice).
• Manages study supplies, devices and drugs, is accountable to the Investigator, sponsor, federal regulatory bodies as per Good Clinical Practice guidelines.
• Provides patient education as per study protocol.
• Identifies, problem-solves, monitors and assesses subjects for adverse events and adherence to protocol under direction of the Investigator.
• Informs investigator, sponsor and UBC Clinical Research Ethics Board of any Serious Adverse Events to patients during the trial.
• Obtains appropriate related study data including blood samples & ECG's, hemodynamic measurements, and angiographic records.
• Case management of ongoing follow-up assessment including history, physical exam, venipuncture, ECG, Doppler ultrasound and other diagnostic tests and counseling of outpatients.
• Completes and corrects study records and case report forms independently or in consultation with the sponsor and/or their representative
• Oversees completion and confidentiality of the study including audits by sponsor and/or regulatory authority.
• Responsible for the overall conduct of the studies and as per Good Clinical Practice.
• Ensures subject safety, regulatory compliance and enrollment expectations are met.
• Meets deadlines for academic and industry sponsors.
• Functions as a resource with hospital staff, patients and colleagues
• Supervises nurses and technologists who are involved with the study conduct or patients.

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