HiRO National Study Coordinator

• Documents 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:

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 one’s own

- Demonstrates a commitment to enhancing one’s own awareness, knowledge, and skills related to equity, diversity, and inclusion

Preferred Qualifications

Bachelor’s 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 University's 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.