Study Start-Up Coordinator– Remote
Lifelancer · Canada · CA
Clinical Research
Remote
physician
Demand72
Career growth70
Healthcare fit72
Remote potential85
5-year outlook
Mid-level CRO regulatory and study start-up roles in Canada typically offer stable compensation with progression toward regulatory lead, start-up lead, or clinical operations management. Exact pay is not stated and will depend on CRO, location, and prior Health Canada submission experience.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-11-09
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- Canada
- Profession fit
- physician
- Rate period
- Annual
Why this was classified this way
- contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians with CRO, Health Canada, and ethics submission experience who want remote clinical operations work. It is less suitable for clinicians without prior clinical research start-up or regulatory experience.
Who should apply
Clinical research coordinators, research nurses, pharmacists, IMGs, or healthcare graduates with CRO exposure and direct experience preparing Health Canada and ethics submissions; bilingual English/French candidates may have an advantage.
CV angle
Frame real clinical research or healthcare experience around regulatory submissions, Health Canada and ethics documentation, ICH-GCP compliance, study start-up timelines, essential document tracking, site communication, and cross-functional collaboration. Do not claim CRO or submission experience unless it is genuine.
Skills to highlight
- Health Canada clinical trial submissions
- Ethics submissions
- ICH-GCP guidelines
- Study start-up coordination
- Essential document management
- Regulatory compliance
- Site communication and tracking
- Bilingual English/French
Role summary
A remote clinical research operations role focused on coordinating study start-up, preparing and filing Health Canada and ethics submissions, tracking essential documents, and advising study teams on regulatory requirements.
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