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Sr. OPHTHALMOLOGY CRA - Canada

  • Toronto, ON, Canada
  • Greater Toronto Area, Canada, Canada

$80 to $85 CAD / hour · Contract

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Job details

Pay
$80 to $85 CAD / hour
Job type
Contract
Apply by
Working hours
25-30 hours per week
Posting language
English
Posted

Original job description

Clinical Research Associate (CRA) - Retina / Ophthalmology | Canada | Contract

About the Opportunity
Our client is seeking a strong-performing Clinical Research Associate to support a portfolio of retina-focused clinical studies in Canada. This role is ideal for an experienced CRA with a solid ophthalmology background who can work independently, manage complex site activities, and keep study execution at a high standard across multiple retina indications.

Key Responsibilities

  • Oversee site monitoring activities across a portfolio of retina-focused studies
  • Ensure protocol compliance and maintain high-quality study execution
  • Manage complex site activities independently
  • Travel to study sites as needed to conduct monitoring visits

Required Qualifications

  • Must be based in Canada
  • Demonstrated proficiency in core CRA responsibilities, with the ability to work independently
  • Ophthalmology experience is required, specifically in retina indications, including:
    • Wet Age-Related Macular Degeneration (Wet AMD)
    • Retinitis Pigmentosa
    • Hyperion studies (all retina-focused)
  • Strong understanding of retina-specific assessments, imaging modalities, and clinical workflows
  • Working knowledge of study protocols and strong attention to detail
  • Excellent organizational skills and comfort in a dynamic, variable-workload environment
  • Willingness to travel to study sites when needed

Engagement Details

  • Duration: 12 months, with extensions likely (these engagements tend to run long)
  • Allocation: Approximately 75% FTE, roughly 25-30 hours per week
  • Location: Remote/hybrid, with about 4-5 days onsite per month. Onsite days may vary by month, and travel is expected to be very minimal in November and December 2026
  • Contract Type: W2 / 1099 / C2C

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.


If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.

More about this job

Responsibilities

Oversee monitoring across retina-focused clinical studies, ensuring protocol compliance and high-quality study execution. Independently manage complex site activities and travel to sites as needed for monitoring visits.

Requirements

Must be based in Canada and have demonstrated CRA experience, the ability to work independently, and ophthalmology experience in retina indications, including Wet AMD and retinitis pigmentosa. Candidates should understand retina-specific assessments, imaging modalities, clinical workflows, and study protocols, and be willing to travel to study sites when needed.

Skills

  • Clinical Site Monitoring
  • Ophthalmology
  • Retina Clinical Research
  • Retinitis Pigmentosa
  • Protocol Compliance
  • Site Management
  • Retina Assessments
  • Ophthalmic Imaging
  • Clinical Workflows
  • Independent Work
  • Attention To Detail
  • Organization
  • Clinical Study Execution

Visa sponsorship

Not detected in the job text

Categories

  • Healthcare
  • Science & Research

Keywords

  • Clinical Research Associate
  • CRA
  • Clinical Research
  • Retina
  • Ophthalmology
  • Retinitis Pigmentosa
  • Hyperion Studies
  • Site Monitoring
  • Clinical Studies
  • Protocol Compliance
  • Study Execution
  • Site Activities
  • Monitoring Visits
  • Retina-Specific Assessments
  • Imaging Modalities
  • Clinical Workflows
  • Study Protocols
  • Canada
  • Contract
  • Remote/Hybrid

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