Hybrid Clinical Trial Associate — Growth & Training

Xenon Pharmaceuticals Inc.

Burnaby

Hybrid

CAD 60,000 - 90,000

Full time

11 days ago
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Benefits offered by this job

Base salary
Target bonus
Stock options
Medical
Dental
Vision
Disability insurance
Life insurance
Employee Assistance Program
Travel insurance
Retirement savings with matching
Vacation
Personal days
Sick days
End-of-year shutdown
Tuition Assistance program

Job summary

Xenon Pharmaceuticals in Vancouver, BC, is looking for a Clinical Trial Associate 1 or 2 to provide support for clinical trials. This hybrid position requires at least two onsite days per week, and it involves assisting with study documentation, regulatory requirements, and project tracking.

The successful candidate will work closely with the Clinical Operations team and is expected to have relevant clinical trial experience in the biotech or pharma industry.

Qualifications

  • 2+ years of relevant experience in pharma/biotech or CRO for Clinical Trial Associate 1.
  • 4+ years of relevant experience for Clinical Trial Associate 2.
  • Knowledge of ICH-GCP guidelines and clinical trial processes.

Responsibilities

  • Support Clinical Operations team with project-specific support related to clinical trials.
  • Review clinical documents and assist with study startup activities.
  • Track key regulatory documents required for site activation.
  • Develop and update clinical trial tracking tools and systems.
  • Collaborate with CROs and clinical sites.

Skills

Clinical trial processes
Project management
Written communication
Oral communication
Microsoft Office

Education

Bachelor’s degree in health sciences

Job description

Xenon Pharmaceuticals in Vancouver, BC, is looking for a Clinical Trial Associate 1 or 2 to provide support for clinical trials. This hybrid position requires at least two onsite days per week, and it involves assisting with study documentation, regulatory requirements, and project tracking.

The successful candidate will work closely with the Clinical Operations team and is expected to have relevant clinical trial experience in the biotech or pharma industry.

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