Posted 7 days ago
Sr. Ophthalmology Clinical Research Associate - Canada
@ SRG
Toronto, Ontario
Overview
SRG, through its client, is hiring a Senior Ophthalmology Clinical Research Associate on a 12-month contract, likely to be extended, to monitor retina-focused clinical studies across Canada. The role involves site monitoring, protocol compliance and managing complex site activities independently. The engagement is remote at about 75% allocation (25-30 hours per week), with 4-5 onsite days per month and travel expected to be minimal in November and December 2026.
Responsibilities:
- Superviser le suivi des sites pour des études axées sur la rétine
- Assurer la conformité au protocole et la qualité de l'exécution
- Gérer de façon autonome les activités complexes des sites
- Se déplacer aux sites d'étude au besoin pour les visites de suivi
Requirements summary:
- Expérience en ophtalmologie, particulièrement en indications rétiniennes
- Expérience avec DMLA humide, rétinite pigmentaire et études Hyperion
- Capacité à travailler de façon autonome
- Solide connaissance des protocoles d'étude et souci du détail
- Disposition à voyager vers les sites d'étude
Tools & skills
Benefits mentioned
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- 2026-11-05
- First seen by our source
- 2026-11-10
- Source record updated
- 2026-11-10
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Allied health |
| Hours per week | 27.5 |
| Travel | air: minimal · ground: moderate |
| Work setting | Home, Client sites |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Encouraged to apply | People with disabilities |
Summary and details written by AI from the posting; the employer’s posting is the authority.
SRG
| Field | Value |
|---|---|
| Open jobs on Jobsy | 1 |
Pharmaceutical 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%, roughly 25-30 hours per week
- Location: Remote, 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 [email protected] or fill out this form to request accommodations.
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