Summary

ZYUS is a Canadian-based life sciences company focused on the global development and commercialization of phyto-therapeutics, such as cannabinoid and protein-based formulations. As an emerging field of medicine, phyto-therapeutics are plant-derived compounds that have been developed for therapeutic use. Through advocacy and research, we intend to deliver high-quality formulations to patients worldwide.

Our aim is to shift the paradigm from the treatment of physical disease to caring for overall well-being, by accelerating the adoption of phyto-therapeutics. We use science as a driver to establish phyto-therapeutics as a standard of care for treating disease & managing the experience of it. To achieve this, we are investing in clinical research, advancing manufacturing, defining scientific standards, delivering high-quality offerings, and raising awareness of medical needs across the industry.

At ZYUS, we are dedicated to expanding the potential of medicine to alleviate human suffering and restore health & well-being – in pursuit of transformational impact on patients.

ZYUS. Advancing the science of well-being.

Join us on our mission.

Your Contribution

  • Support the development of company’s clinical/pre-clinical research initiatives.
  • Maintain the technical and scientific research aspects of clinical trials, including internal cross-functional clinical research affairs and external research organizations (CROs, clinical trial sites, and vendors).
  • Support collaborative clinical partners with emphasis on assigned clinical trial sites.
  • Work closely with interdisciplinary teams of internal and external researchers, clinicians, project managers, and regulatory entities to ensure proper execution of clinical trials.
  • Contribute to clinical trial protocol writing/review, method validation research, and feasibility assessments in collaboration with interdisciplinary teams of researchers, clinicians, and medical writers.
  • Participate in the authorship and review of clinical study amendments, consent forms, case report forms, and other clinical study documents (IND/CTA) in collaboration with cross-functional study teams, as directed.
  • Support the clinical data screenings, data analyses, and study documentations.
  • Ensure timely delivery of pre-clinical data review and assist with periodic review of study files for completeness.
  • Assist in development of evidence portfolio, including writing journal publications and summary articles, and technical clinical documents.
  • Research, review and analyze the literature as directed.

What it Takes

  • PhD plus 5+ years of work experience in Health and Life Sciences.
  • Strong research record and demonstrated experience in independent research design and implementation.
  • Ability to plan, develop, and execute early clinical development studies including analysis, interpreting, and reporting results as directed.
  • Demonstrate a record of innovation and development, and publications.
  • Ability to meet high-performance standards and productivity requirements in a fast-paced team environment.
  • Able to initiate and participate in cross-functional teams to support programs diverse in disease and modalities as directed.
  • A strong collaborative, communicative and problem-solving disposition is essential.

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 careers@zyus.com.