Source Data Verification (SDV) jobs

FSP Sr Clinical Research Associate I

Thermo Fisher Scientific · Posted Nov 12, 2026

Thermo Fisher Scientific · Posted Nov 12, 2026

Fortrea · Posted Nov 11, 2026

Clinical Research Associate responsible for site monitoring, data integrity, and regulatory compliance for clinical trials in Beijing.

Conduct site monitoring visits including pre-study, initiation, routine, and close-out
Verify study training records and informed consent procedures
Review source documents and generate queries
Maintain eTMF and sponsor documents
Track investigational product inventory

University or college degree, or certification in a related allied health profession
Nice to have: Phase I monitoring experience
Nice to have: Life Science or Nursing qualification
Nice to have: Fortrea SOPs knowledge
Nice to have: additional years in related field

Thermo Fisher Scientific · Posted Nov 6, 2026

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

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

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

Thermo Fisher Scientific · Posted Nov 6, 2026

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

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

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