Neuroscience-Jobs in Kanada

Xenon Pharmaceuticals (NASDAQ:XENE) is a neuroscience-focused biopharmaceutical company committed to discovering, developing, and commercializing innovative therapeutics to improve the lives of people living with neurological and psychiatric disorders. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team.

We are advancing an exciting product pipeline to address indications with high unmet medical need, including epilepsy and depression. Our flagship azetukalner program is the most advanced potassium channel modulator in clinical development for multiple indications. Building on positive results from our Phase 2b “X-TOLE” study in adult patients with focal epilepsy, our Phase 3 epilepsy program includes multiple trials evaluating azetukalner for focal onset seizures and primary generalized tonic-clonic seizures. In 2024, we plan to initiate a Phase 3 program in major depressive disorder, based on topline data from our Phase 2 “X-NOVA” trial. Additionally, our discovery labs are engaged in early-stage research leveraging our ion channel expertise to identify new drug targets and develop novel candidates. Supported by a strong balance sheet, we aim to build a fully integrated, leading neuroscience company with capabilities across discovery, clinical development, and commercial operations.

We are seeking a Clinical Trial Associate 1 or 2 to support our Clinical Operations team. The role involves assisting with project-specific activities related to clinical trial conduct, ensuring efficient study execution through administrative and tracking support. This position reports to the Senior Director, Trial Operations, based in Vancouver, BC, Canada. The level (Associate 1 or 2) will depend on the candidate’s education and experience. It is a hybrid role requiring at least 2 days per week in the office.

1. Review clinical documents (protocols, consent forms, study plans). Participate in study start-up activities, including preparing reference manuals, site tools, templates, and guidelines.
2. Coordinate with CROs, vendors, and sites for trial activities such as sample management, shipment, and distribution of supplies.
3. Assist with regulatory document review and tracking for site activation, including consent forms.
4. Develop and maintain clinical trial tracking systems to monitor progress, recruitment, and supplies.
5. Support the trial master file management, including electronic filing and quality oversight of CRO eTMF.
6. Process invoices and payments related to the trial.
7. Assist with meeting logistics, including scheduling, preparing agendas, and documenting minutes.
8. Coordinate sample shipments, track receipt, and prepare reports.
9. Monitor timelines, budgets, and trial materials.
10. Assist in planning Investigator meetings and regulatory audits.
11. Perform quality control reviews of study documents and SOPs.
12. Participate in process improvement projects.
13. Gain understanding of clinical research protocols and regulations.
14. Adhere to company policies and ethical standards.
15. Perform other duties as assigned.

• Bachelor’s degree in health sciences or related field.
• For Associate 1: 2+ years of relevant experience in pharma/biotech or CRO, or equivalent education/experience.
• For Associate 2: 4+ years of relevant experience.
• Knowledge of clinical trial processes and ICH-GCP guidelines.
• Strong organizational, communication, and computer skills.
• Ability to manage multiple projects and work independently and collaboratively.
• Interest in clinical research and willingness to learn.

The salary range for this role is $58,750 to $81,475 CAD. We consider above-range offers for exceptional candidates. Our Total Rewards include salary, bonus, stock options, and comprehensive benefits. We promote a healthy work-life balance and support employee development through various programs.

Note: US positions participate in E-Verify. Finalists will undergo background checks.

To apply, click "Apply Now". We appreciate all applicants; only selected candidates will be contacted.