Senior Clinical Research Associate | REMOTE (Remote, United States)
Sonova Group · United States · US
Clinical Research
Remote/Hybrid — check advert
Nurse
Dentist
Demand78
Career growth72
Healthcare fit78
Remote potential60
Salary band
USD 91k – 114k
5-year outlook
Senior CRA skills remain in demand in medtech and pharma, with progression toward Clinical Trial Manager or Clinical Operations Lead. Pay is likely competitive but varies by geography, device versus pharma setting, and travel requirements.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-24
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Nurse, Dentist
- Rate period
- Annual
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 if you already have CRA/site-monitoring experience and want a remote medtech clinical operations role. Clinicians without independent monitoring experience are unlikely to clear the senior bar.
Who should apply
Experienced CRAs with 5+ years in clinical research and independent site monitoring, especially nurses, pharmacists, allied health professionals, or doctors with GCP and site management experience. Class III device or global multicenter trial experience is a plus.
CV angle
Frame real clinical/research work as site management and trial operations: number and types of sites, monitoring visits, enrollment, protocol deviations, data queries, TMF/eTMF, audit/inspection preparation, and cross-functional work with data, regulatory, and quality teams. For clinicians, translate patient-care experience into GCP compliance, adverse event reporting, investigator communication, and data quality without claiming CRA duties you did not perform.
Skills to highlight
- Site monitoring (SQV/SIV/IMV/COV)
- ICH-GCP and ISO 14155
- FDA regulations and clinical trial compliance
- CTMS, EDC, and eTMF
- Site activation and enrollment management
- Risk mitigation and protocol deviation management
- Audit/inspection readiness
- Cross-functional collaboration and CRA mentoring
Role summary
Senior CRA leads operational execution of global medical device clinical studies, managing investigative sites, monitoring visits, study quality, regulatory documentation, risk mitigation, and cross-functional trial activities from start-up to close-out.
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