Sr. OPHTHALMOLOGY CRA - Canada

SRG

Canada

Hybrid

CAD 52,000 - 76,000

Full time

5 days ago
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Job summary

SRG seeks a Clinical Research Associate to support retina-focused trials across Canada. The candidate will manage site monitoring, ensure protocol compliance, and coordinate activities across multiple retina indications.

The role is remote/hybrid with about 4–5 onsite days per month, lasting 12 months with extensions likely. It is approximately 75% FTE (roughly 25–30 hours per week). Travel to sites will be required as needed.

Qualifications

  • Must be based in Canada.
  • Ophthalmology experience, retina indications (wet AMD, Retinitis Pigmentosa).
  • Strong understanding of retina assessments and clinical workflows.
  • Willingness to travel and work independently.
  • Duration: 12 months with potential extensions; 75% FTE (~25–30 hours/week).
  • Remote/hybrid with 4–5 onsite days per month; November/December 2026 travel minimal.

Responsibilities

  • Oversee site monitoring across retina-focused studies in Canada.
  • Ensure protocol compliance and high-quality study execution.
  • Manage complex site activities independently.
  • Travel to study sites as needed for monitoring visits.

Skills

Independent worker
retina experience
Clinical monitoring
Attention to detail

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
  • 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.

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