Clinical Research Associate II
ICON · United States · US
Clinical Research
Remote
Dentist
Demand78
Career growth72
Healthcare fit72
Remote potential35
5-year outlook
CRA II compensation generally progresses with monitoring experience and CRO scale, with pathways toward senior CRA, clinical trial management, or study leadership roles. Exact pay varies significantly by country, travel load, and prior CRA experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
mid
Employment type
full-time
Date found
2026-11-05
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- 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 considering if you already have CRA monitoring experience or strong clinical research site experience plus ICH-GCP knowledge. Clinicians without prior CRA experience may find the 2-year CRA requirement and 60% travel a significant barrier.
Who should apply
Research nurses, clinical research coordinators, pharmacists or doctors with CRO/site monitoring exposure, and healthcare professionals who already have at least 2 years of CRA experience and want a CRO-based clinical research career.
CV angle
Frame real experience around trial monitoring, site coordination, ICH-GCP compliance, protocol adherence, patient safety, data review, query resolution, and study documentation. Quantify sites supported, monitoring visits, query volumes, or study complexity where possible, and do not claim CRA experience unless it is genuine.
Skills to highlight
- Clinical trial monitoring
- ICH-GCP compliance
- Site qualification, initiation, and close-out visits
- Protocol compliance and patient safety
- Data review and query resolution
- Clinical study documentation
- Investigator and site staff communication
- Organizational and travel-based site management
Role summary
A CRO-based Clinical Research Associate II role focused on monitoring clinical trial sites, ensuring protocol compliance and data integrity, resolving data queries, and supporting study documentation across investigator sites.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.