HiRO National Study Coordinator

Job Category

Job Profile

Job Title

Department

Compensation Range

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 the normal course employees will be hired transferred or promoted between the minimum and midpoint of the salary range for a job.

Posting End Date

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

Job End Date

This is a leave replacement for a 1-year term duration.

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
Heart in Rhythm Organization (HiRO) National Study Coordinator

Organizational Status
Reporting directly to Dr. Andrew Krahn and Dr. Zachary Laksman. Liaison with National HiRO coordinator finance and biobank coordinator and UBC and recruiting site coordinators.

Work Performed

• Writes standard protocols and procedures for the UBC cardiogenetics research program ( research protocols consents/assents and pertaining documents for research ethics board (REB) review

• Coordinates the process of ethics submissions and maintenance of certification for research studies clinical trials grants and sub-studies

• Drafts patient consent forms

• Ensures regulatory documents are in order and updated as necessary

• Coordinates contracts for studies and oversees data/sample sharing for the program (including 25 enrolling sites nationally)

• Writes materials for research reports for assigned projects as appropriate for funding agencies and donors

• Coordinates logistics of study protocols with hospital departments i.e. lab radiology OR etc.

• Fosters and manages relationships between the scientific and operational teams of research projects and central UBC business units such as Human Resources Supply Management Payroll and Research Finance.

• Communicates with and supports site investigators and coordinators collaborating in multicenter projects including clinical trials

• Develops background materials and liaises with committee and study team members

• Supports HiRO patient engagement and knowledge translation initiatives

Consequence of Error/Judgement

Lack of careful attention to regulatory guidelines and approvals could suspend Investigator/physician and hospital/University as a site for further clinical research and/or funding. The performance of research projects must strictly conform to appropriate regulations:

1) personal: maintaining professional behavior and respect for subjects and staff 2) local: the UBC Clinical Research Ethics Board 3) Provincial: B.C. Privacy Act and 4) The University of British Columbia (UBC) Office of Biobank Education and Research (OBER)and CTRNet () 5)Federal: Health Canada International Conference on Harmonization Tri-Council Policy Statement Good Clinical Practice.

Supervision Received
Works independently. Reports to the PIs.

Supervision Given
May give direction and training to other staff and students.

Minimum Qualifications
Undergraduate degree in a relevant discipline. Minimum of two years of related experience or an equivalent combination of education and experience.

- Willingness to respect diverse perspectives including perspectives in conflict with ones own

- Demonstrates a commitment to enhancing ones own awareness knowledge and skills related to equity diversity and inclusion

Preferred Qualifications

Bachelors degree or recognized equivalent in a health or science-related discipline. Minimum of three years experience or the equivalent combination of education and experience. Experience in research planning/facilitation and clinical trials preferred. Familiarity with ethical legal and regulatory requirements in an academic research setting. Training and certification in ICH/GCP guidelines (ACRP or SOCRA) are preferred and certification with experience in the CIHR Strategy for Patient-Oriented Research -Patient Engagement Framework (SPOR) as well as Knowledge Translation are considered a valuable asset.

Ability to analyze and interpret data determine implications and provide recommendations. Excellent project management skills with strong analytical and problem-solving skills. Experience working in a research-intensive University is preferred; experience working in a large and complex institutional environment is an asset. Proven ability to develop credibility and effective working relationships with faculty staff and other relevant stakeholders. Knowledge of UBC policies and procedures and an understanding of the Universitys organizational structure and governance. Excellent written and verbal communications skills. Ability to take complex scientific information and translate into clear and succinct language for a broader audience. Demonstrated ability to be thorough accurate and have a high level of attention to detail. Ability to effectively manage multiple tasks and priorities. Ability to exercise tact and discretion when handling confidential and sensitive information.