Senior Clinical Research Associate (Pool)
Vanguard Clinical · United States · US
Clinical Research
Remote
Not yet analysed
Demand72
Career growth65
Healthcare fit64
Remote potential15
Salary band
USD 120k – 145k
5-year outlook
Senior CRA compensation is generally competitive within clinical research and CRO markets, with stability tied to monitoring experience, therapeutic area demand, and sponsor budgets. Exact salary varies by region, travel load, and employer.
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
- 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 for experienced CRAs or clinicians with substantial clinical monitoring experience who want a site-facing CRO role. It is less suitable for clinicians without prior monitoring experience because of the senior experience bar and high travel requirement.
Who should apply
Experienced Clinical Research Associates, research nurses or coordinators with independent monitoring exposure, and doctors or pharmacists with strong clinical trial site experience seeking a CRO monitoring role.
CV angle
Frame real clinical trial site experience around independent monitoring activities, ICH/GCP compliance, site qualification/initiation/interim/closeout support, TMF/eTMF maintenance, query resolution, patient safety, data integrity, and sponsor/site communication. Quantify sites, visits, therapeutic areas, and compliance outcomes only where genuinely true; do not claim independent CRA monitoring experience if it was not performed.
Skills to highlight
- Clinical monitoring
- ICH/GCP compliance
- Site management
- TMF/eTMF maintenance
- Query resolution
- Phase 1-3 clinical trials
- Patient safety and data integrity
- Sponsor and site communication
Role summary
A senior CRA role responsible for independently monitoring clinical trial sites, conducting qualification/initiation/interim/closeout visits, maintaining TMF/eTMF records, resolving queries, and ensuring ICH/GCP and sponsor compliance across Phase 1-3 trials.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.