Clinical Research Assistant Jobs

Clinical Research Assistant

ZYUS is a Saskatoon-based life sciences company focused on the global development and commercialization of cannabinoid-based pharmaceutical drug product candidates and innovative exempt market therapeutics. Through clinical research, ZYUS is committed to furthering the understanding of cannabinoids with the clinical development of its pharmaceutical drug product candidates and intellectual property activities to protect its novel formulations. Additionally, ZYUS is dedicated to delivering high quality, cGMP / EU GMP-compliant cannabinoid products to patients through the exempt global medical market.

The ZYUS vision is to elevate cannabinoid-based therapeutics as a standard of care and expand the potential of protein-based formulations in pursuit of a transformational impact on patients’ lives around the world.

ZYUS. Advancing the science of well-being.

Join us on our mission.

Summary of Key Responsibilities (job functions include but are not limited to):

Reconcile differences amongst regulatory guidance to inform decision-making for discovery, preclinical/nonclinical and clinical studies.

Review of the literature and regulatory information to inform scientific decision-making.

Update literature and clinical trials search tables.

Assist the team with the review of clinical findings, systematic review of the related literature and clinical trials to support the company’s drug development plan.

Assist the clinical team in preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.

Assess overall filing, documentation, reporting and archiving process on ongoing basis for clinical trial activities.

Assist with periodic review of study files for completeness.

Archiving clinical research documents.

Tracking and maintenance of any correspondence with Clinical Research Organizations (CROs) or collaborative partners.

Assist Clinical Research Associates (CRAs) with preparation, handling and distribution of Clinical Trial information, supplies, and maintenance of tracking information.

Assist in implementing process improvements.

Assist in clinical trial correspondence.

·Attend regular meetings as required.

Qualifications/Requirements:

·Bachelor’s degree (BSc) in a health-related discipline.

·1+ years of experience working in a research-based environment.

·Master’s degree would be considered an asset.

Benefits of Joining Our Team

At ZYUS, we care about our people. Our total rewards package includes comprehensive benefits, retirements savings, paid time off, on-going training and development opportunities.

We would like to thank all applicants in advance for submitting their resumes. Please note, only those candidates chosen to continue on through the selection process will be contacted.