Research Assistant: Clinical Studies & Regulatory Support

UM Careers; Winnipeg; On-site; CAD 42,000 - 61,000; Full time

Job summary

University of Manitoba is seeking a research staff member to support regulatory submissions, document maintenance, and project coordination for clinical studies. The role emphasizes compliance with ICH-GCP, TCPS2, and Health Canada guidelines while collaborating closely with cross-functional teams.

The position requires a university degree in a related field and strong English communication skills, with prior research experience preferred.

Qualifications

• University degree in related field, including laboratory analysis techniques, is required.
• Previous research experience is preferred.
• Knowledge of Good Clinical Practice guidelines, PHIA and TCPS2 is preferred.

Responsibilities

• Complete regulatory submissions and coordination of site submissions.
• Maintain regulatory documents.
• Ensure compliance with ICH-GCP, TCPS2, FIPPA/PHIA, Health Canada rules and institutional policies.
• Manage day-to-day tasks of research projects including research charts.
• Assist with monitoring visits and data collection.
• Liaise with departments to support research activities and collaborate with team.
• Provide back-up support to team members as required.
• Adhere to safety and health policies and safe work practices.

Skills

Interpersonal skills

English proficiency

Teamwork

Time management

Microsoft Office

Education

University degree

Tools

Microsoft Office

Outlook

PowerPoint

Excel

Job description

University of Manitoba is seeking a research staff member to support regulatory submissions, document maintenance, and project coordination for clinical studies. The role emphasizes compliance with ICH-GCP, TCPS2, and Health Canada guidelines while collaborating closely with cross-functional teams.

The position requires a university degree in a related field and strong English communication skills, with prior research experience preferred.