Clinical Research Associate II — Monitoring & Site Management

ThermoFisher Scientific; Guilford (CT); On-site; USD 70,000 - 110,000; Full time

Job summary

Thermo Fisher Scientific is seeking a CRA (Level II) to coordinate clinical monitoring and site management. Duties include on-site and remote visits, data verification, regulatory compliance, and collaboration with sponsors. Travel will exceed 75% to ensure protocol adherence and data integrity.

The role requires a life sciences degree or RN certification with monitoring experience and strong communication skills in English.

Qualifications

• Bachelor’s degree in a life sciences field or RN certification with related experience.
• 1+ years of clinical research monitoring experience or equivalent.
• Valid driver’s license where applicable.

Responsibilities

• Monitors investigator sites using risk-based monitoring approaches.
• Performs data review activities (SDR/SDV/CRF) during on-site or remote visits.
• Documents findings promptly and escalates issues to clinical management.
• Maintains trial documentation and ensures regulatory compliance.
• Travel requirement >75% as part of role.

Skills

Clinical monitoring

Regulatory knowledge

ICH GCP familiarity

Root cause analysis

Excellent written & verbal English

Critical thinking

Time management

Education

Bachelor’s degree in life sciences

Registered Nursing (RN) certification

Tools

MS Office

Job description

Thermo Fisher Scientific is seeking a CRA (Level II) to coordinate clinical monitoring and site management. Duties include on-site and remote visits, data verification, regulatory compliance, and collaboration with sponsors. Travel will exceed 75% to ensure protocol adherence and data integrity.

The role requires a life sciences degree or RN certification with monitoring experience and strong communication skills in English.