Job Details


ZYUS is a Canadian-based, next-generation life sciences company leading scientific research and development in phyto-therapeutics. We are committed to delivering high-quality standardized therapeutic formulations that comply with Good Manufacturing Practices (GMP) to provide targeted relief for our patients.

We aim to shift the paradigm from conventional strategies to focus on improving our patients’ overall quality of life and well-being by harnessing the power of cannabinoids. With science as our driver, we can reimagine the potential of phyto-therapeutics by investing in medical research, clinical trials, and advanced process manufacturing. Together, we can establish phyto-therapeutics as a standard of care to restore health and manage disease.

At ZYUS, we are forging a new industry of phyto-therapeutics by elevating cannabinoid formulations as a standard of care and reimagining the potential of protein-based formulations – in pursuit of transformational impact on patient lives.

ZYUS. Advancing the science of well-being.

Join us on our mission.

Your Contribution

  • Develop a study management plan under the supervision of the Director of Clinical Research and CRO representative(s), outlining target KPIs, risk assessment, and contingency planning. 
  • End-to-end management of clinical studies to ensure appropriate resourcing and timely, highquality delivery by all functional areas. Ability to identify and organize resources and services needed to accomplish tasks, set objectives, plan for contingencies, and managing time effectively.
  • Assist in screening, selection, and management of CROs and vendors in accordance with contractual timelines, sponsor specifications, quality, budget, and GCP.
  • Develop and monitor study metrics to continuously assess study progress.
  • Act as the primary point of contact between ZYUS and CRO project team(s).
  • Monitor and track study status, timelines, and budget expenditures; identifies opportunities and recommend implementation plans for efficiency measures.
  • Ensures timely data entry, query resolution and prompt resolution of data issues.
  • Accountable for review of study budget, expense reports and financial records (invoicing/units/expenses) in conjunction with appropriate project team members.
  • Manage the current or future clinical research coordinators and their activities on each study.
  • Ensure that study activities (personal and those of the Clinical Research team) are properly tracked and entered into the company’s time tracking/project management/resource planning software tool in a timely manner.
  • Contribute to the study-specific audits of the clinical trial activities.
  • Collaborate with internal and external multidisciplinary teams for ZYUS clinical trial regulatory submissions.
  • Accountable for development, oversight, and delivery of team training for specific projects.
  • Applies expertise in day-to-day clinical operations activities, collaborate with internal and external cross-functional team members to develop study documents and manuals, including protocols, ICFs, manuals, presentation decks, risk plans, etc.
  • Conduct performance reviews, calibration sessions and feedback discussions for the current or future clinical research coordinators. Perform competency assessments across his/her team and implements and monitors development plans with direct reports.
  • Manage performance of external service providers as required.

What it Takes

  • Bachelor’s degree in Health Sciences required. Advanced degree or equivalent clinical research experience preferred. Post-secondary or certificate in project management is considered an asset.
  • 8+ years clinical research experience including project management and experience in clinical trial operations; or equivalent combination of education, training and experience.
  • Excellent knowledge of ICH/GCP.
  • Advanced proficiency in project management tools to streamline the workflow.

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 thank all the applicants; only those selected for an interview will be contacted. To apply, please email a copy of your resume to