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1–2 jobs· newest first

Sr. Clinical Research Associate - Early Phase Studies
Thermo Fisher Scientific · Austin, US+1 more
Senior
Sr. Clinical Research Associate - Early Phase Studies
Thermo Fisher Scientific · Las Vegas, US
On-site · Full-time · Mid

+10K new in the last hour

Sr. Clinical Research Associate - Early Phase Studies

Thermo Fisher Scientific · Posted Nov 6, 2026

Austin, Texas, United States +1 more
Senior
3+ years

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Clinical Research Associate supporting early‑phase clinical trials, primarily at investigational sites in Austin, Texas and Las Vegas, Nevada.

Locations (2)

Austin, Texas, United States
Las Vegas, Nevada, United States

Responsibilities

Independently monitor investigational sites using risk‑based monitoring
Conduct site qualification, initiation, interim monitoring and close‑out visits
Support Phase I and early‑development studies including complex pharmacology protocols
Perform source data review, verification and CRF review
Assess investigational product accountability

Requirements

Bachelor's degree in life sciences, nursing, pharmacy, or a related medical/scientific discipline
Nice to have: First‑in‑Human (FIH)
Nice to have: Single Ascending Dose (SAD)
Nice to have: Multiple Ascending Dose (MAD)
Nice to have: PK/PD studies

Skills

clinical monitoring site qualification site initiation interim monitoring close‑out visits risk‑based monitoring source data review source data verification CRF review investigational product accountability protocol compliance ICH‑GCP guidelines regulatory requirements clinical data review

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Sr. Clinical Research Associate - Early Phase Studies

Thermo Fisher Scientific · Posted Nov 6, 2026

Las Vegas, Nevada, United States
On-site
Full-time · Mid
3–5 years

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Clinical Research Associate supporting early-phase clinical trials at a primary investigational site in Las Vegas, Nevada.

Responsibilities

Independently monitor investigational sites using risk-based monitoring
Conduct site qualification, initiation, interim monitoring, and close-out visits
Support Phase I and Early Development studies including complex pharmacology protocols
Monitor early-phase study activities with focus on safety and dose escalation
Perform source data review and verification

Requirements

Bachelor's degree in life sciences, nursing, pharmacy, or a related medical/scientific discipline
Nice to have: experience with complex early-phase protocols
Nice to have: lead CRA experience
Nice to have: mentoring junior CRAs
Nice to have: independent work in lean or cross-functional structures

Skills

clinical monitoring site qualification site initiation interim monitoring close-out visits

clinical pharmacology protocols

dose escalation procedures

safety monitoring

audit readiness

Microsoft Office

clinical trial management systems (CTMS)

risk-based monitoring

source data review

source data verification

clinical pharmacology protocols

Single Ascending Dose

Multiple Ascending Dose

drug-drug interaction

bioavailability

clinical trial management systems

Microsoft Office

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