Sr. Clinical Research Associate - Early Phase Studies (Las Vegas, NV)
Thermo Fisher Scientific · Las Vegas, Nevada, USA · Global
Clinical Research
–
Not yet analysed
Demand70
Career growth65
Healthcare fit62
Remote potential20
5-year outlook
Senior CRA compensation in large CROs is generally stable to modestly growing, with early-phase/Phase I units often paying at or above general CRA bands due to intensity and shift demands. Salary details are not stated in this posting — verify against current CRO benchmarks rather than assuming.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
–
Date found
2026-11-09
Intelligence details
Flexible work details
- Eligible countries
- United States
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 or site research coordinator experience and want a large-CRO early-phase role; clinicians with purely bedside backgrounds should expect a hard screen at the senior level and may need to target CRA I/II or site-side roles first.
Who should apply
Experienced CRAs seeking early-phase exposure at a large CRO; research nurses or clinical research coordinators with Phase I unit experience; pharmacists or doctors who have worked on investigator-initiated or industry trials and can evidence monitoring-adjacent duties.
CV angle
Reframe real clinical work into research language: protocol adherence, eligibility screening, informed consent process, adverse event and SAE reporting, source documentation accuracy, investigational product handling and accountability, regulatory binder upkeep, and ICH-GCP compliance. Quantify trial or audit exposure (number of studies, participants screened/enrolled, monitoring or audit findings resolved) only where true — do not claim monitoring visits you have not performed.
Skills to highlight
- ICH-GCP and protocol compliance
- Site monitoring and source data verification
- Informed consent process
- Adverse event / SAE reporting
- Clinical documentation accuracy
- Regulatory and essential document management
- Phase I / early-phase trial exposure
- Cross-site and sponsor communication
Role summary
A senior monitoring role at Thermo Fisher Scientific's clinical research organization, overseeing early-phase (Phase I) trial sites in Las Vegas: conducting qualification, initiation, monitoring and close-out visits, verifying source data against case report forms, and ensuring protocol, ICH-GCP and regulatory compliance. Exact duties are inferred from the title, as no description was supplied.
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