Senior Clinical Research Associate - Global Trials

ThermoFisher Scientific; United States; Hybrid; USD 70,000 - 110,000; Full time

Job summary

Thermo Fisher Scientific in the United States is seeking a Clinical Research Associate to monitor trial sites, ensure protocol and regulatory compliance, and safeguard patient safety and data integrity across studies.

The role involves on-site and remote monitoring, site management, RBM, and collaboration with sponsors and cross-functional teams, with travel requirements and a focus on quality and audit readiness.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, or related field, or equivalent.
• Valid driver's license, where applicable.
• Ability to travel as required.

Responsibilities

• Conduct on-site and remote monitoring visits using risk-based monitoring.
• Review source documentation and case report forms for accuracy and completeness.
• Perform site management activities including initiation, monitoring, and close-out visits.
• Assess investigational product accountability through inventory reviews.
• Identify process issues and support corrective actions.
• Ensure essential documents meet ICH-GCP and regulatory requirements.
• Prepare monitoring reports and study documentation within timelines.
• Maintain communication with sites, sponsors, and study teams.
• Support RBM, site feasibility, and investigator engagement where applicable.

Skills

ICH-GCP knowledge

RBM experience

Medical terminology understanding

Organizational skills

Communication skills

MS Office proficiency

CTMS familiarity

English proficiency

Travel readiness

Education

Bachelor’s degree in Life Sciences or related field

Tools

CTMS software

Microsoft Office Suite

Job description

Thermo Fisher Scientific in the United States is seeking a Clinical Research Associate to monitor trial sites, ensure protocol and regulatory compliance, and safeguard patient safety and data integrity across studies.

The role involves on-site and remote monitoring, site management, RBM, and collaboration with sponsors and cross-functional teams, with travel requirements and a focus on quality and audit readiness.