Source Nutraceutical jobs

SOURCE NUTRACEUTICAL, INC.

Winnipeg, MB, CANADA R3T 1T4

Source Nutraceutical, Inc. (SNI) is a fast-growing company with offices in Winnipeg, Manitoba and Toronto, Ontario. The company is an integrated “one-stop shop” for regulatory affairs, clinical research, quality assurance, packaging and labeling compliance, marketing support, and fulfillment needs. We have a substantial client base that is constantly growing.

SNI offers the opportunity to further professional development and technical expertise. We provide competitive wages and benefits, free parking, and more. We offer an environment that is team-oriented and focused on continuous improvement!

The casual position of Clinical Research Assistant reports to the Director of Clinical Affairs and Regulatory Strategy, and is responsible for clinical trial operations. This position will be an in-person role at our corporate headquarters in Winnipeg, Manitoba.

The Clinical Research Assistant will be responsible for facilitating the ethical conduct of a Clinical Trial (CT) involving human participants under the supervision of the study Principal Investigator (PI) and CT Operations Manager. This responsibility includes adhering to approved study protocols, applicable regulatory and research ethics requirements, and Good Clinical Practice (GCP) standards.

Responsibilities:

• Review and maintenance of a working knowledge of company Standard Operating Procedures (SOPs); all study-specific protocols; and relevant clinical trial guidelines from ICH (International Council for Harmonisation) GCPs, Health Canada, and U.S. FDA (Food and Drug Administration).
• Completing all required training relevant to CT operations (i.e., study-specific equipment procedures); the Personal Health and Information Act (PHIA); research ethics (TCPS Core-II); and ICH-GCP guidelines.
• Completing study procedures while ensuring compliance with the study protocol.
• Ensuring the proper handling, dispensing, application, and storage of the study test articles.
• Collecting study data and completing source documentation in accordance with protocol requirements and SOPs, ensuring accuracy and completeness.
• Maintaining participant documentation logs while adhering to CT confidentiality best practices.
• Completing other duties as assigned as required by Management and as training/experience allows.

Position Requirements and Experience:

• University graduate (or current University graduate student) in Human Health and Nutrition; Biological Science; Biotechnology; Food Science; or a related discipline.
• Proficiency with Microsoft Word, Excel, Powerpoint and Outlook.
• A high standard of accuracy and attention to detail.
• Strong inter-personal skills.
• The ability to work as a member of a team in a timeline-driven environment.
• Excellent written and oral communication skills.
• A positive working attitude.
• The ability to thrive in an environment of growth and change.
• Eligibility to work in Canada.
• Candidate must be available to work on-site at our corporate headquarters (Winnipeg, Manitoba).

Assets:

• Additional education and/or professional certifications would be an asset, including: Master of Science (MSc) degree. / Certified Clinical Research Coordinator (CRC).
• Experience with clinical trial project coordination, operations, and/or data management.
• Knowledge and/or experience in working with a clinical trial management system (CTMS), e-consent processes, and electronic data capture (EDC).

If you are passionate about the clinical trial industry in support of new product commercialization, then this position may be for you!

Please send your resume to humanresources@sourcenutra.com before November 6, 2026.

We thank those who apply, however only qualified applicants will be contacted.

Requirements

• Required: Practical data collection, data management, research, and medical terminology skills, with careful record keeping, clear communication, and the ability to follow study procedures. Preferred: clinical trial operations, analysis skills, and supervising experience that support participant care, thoughtful review of information, and effective coordination with research teams.

Expected hours: No more than 25.0 per week

Benefits:

• Flexible schedule
• On-site parking

Work Location: In person