Clinical Research Coord I

University of South Florida; Canada; On-site; CAD 50,000 - 70,000; Full time

Job summary

A leading educational institution in Canada is seeking a Clinical Research Coordinator I to support the coordination of clinical research activities. The role involves participant enrollment, data collection, and collaboration with study teams. Ideal candidates should have a Bachelor's degree and experience in clinical settings. This position is grant funded and requires compliance with all relevant regulations.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.

Responsibilities

• Coordinate and perform assigned clinical research activities and study visits.
• Assist in participant screening, enrollment, and retention to ensure study milestones are met.
• Conduct and document study procedures such as vital signs, ECGs, and biological sample collection.
• Communicate and collaborate with investigators, clinical teams, and study sponsors.
• Assist with regulatory submissions, monitoring visits, and audits.
• Maintain study documentation and research materials.
• Ensure compliance with study protocols and regulations.
• Provide support to junior research staff.

Education

Bachelor's degree in a related field

Job description

Job Description

The Clinical Research Coordinator I supports the coordination and implementation of clinical research activities within the Department of Obstetrics and Gynecology. This role involves assisting principal investigators and lead coordinators with study procedures, participant enrollment, data collection, and ensuring compliance with study protocols and regulatory requirements. This position is grant funded.

Responsibilities

• Coordinate and perform assigned clinical research activities and study visits.
• Assist in participant screening, enrollment, and retention to ensure study milestones are met.
• Conduct and document study procedures such as vital signs, ECGs, and biological sample collection per protocol.
• Communicate and collaborate with investigators, clinical teams, and study sponsors.
• Assist with regulatory submissions, monitoring visits, and audits.
• Maintain study documentation, inventory, and research materials.
• Ensure all research activities comply with study protocols, institutional policies, HIPAA, and applicable regulations.
• Provide support and guidance to junior research staff as needed.

Qualifications

Bachelor's degree in a related field -OR- equivalent combination of education and experience.

Compliance and Federal Notices

This position may be subject to a Level 1 or Level 2 criminal background check.

Applicants have rights under Federal Employment Laws.

Equal Employment Opportunity

The University of South Florida is an equal opportunity employer that does not discriminate against any employee or applicant for employment based on any characteristic protected by law. The University maintains affirmative action programs for protected veterans and individuals with disabilities in accordance with all applicable federal and state laws. This job description does not constitute an employment contract.