Experienced CRA 1 or 2 - Unblinded - West Coast (California, Oregon, Arizona,
Lifelancer · United States · US
Clinical Research
Remote
Nurse
allied_health
Demand72
Career growth66
Healthcare fit68
Remote potential35
5-year outlook
CRA compensation generally grows with monitoring experience, sponsor/CRO complexity, and therapeutic-area expertise, but this FSP role's heavy travel and contract structure may affect stability. Exact salary is not stated.
Clinical license
Not required
Applicant reach
narrow
Seniority
junior
Employment type
full-time
Date found
2026-11-09
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Nurse, allied_health
- 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 considering if you already have CRA monitoring experience and can handle frequent overnight travel; less suitable for clinicians seeking a fully remote, entry-level transition without prior monitoring exposure.
Who should apply
Nurses, allied health professionals, clinical research coordinators, IMGs, or healthcare graduates with 1-3 years of site monitoring experience who live in the specified West Coast/Texas markets and are comfortable with heavy travel.
CV angle
Frame real clinical experience around protocol adherence, informed consent, source documentation, adverse event/SAE reporting, data quality and query resolution, regulatory compliance, site communication, and co-monitoring/training where genuinely applicable.
Skills to highlight
- Clinical site monitoring
- Source document verification
- Informed consent and protocol compliance
- SAE reporting and safety follow-up
- CRF review and query resolution
- Regulatory/GCP compliance
- Site management and communication
- Electronic data capture systems
Role summary
An FSP Clinical Research Associate monitors clinical trial sites, verifies protocol and informed consent compliance, reviews source data and CRFs, supports SAE reporting, and coordinates site management with substantial onsite and overnight travel.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.