Senior Clinical Research Associate I — On-Site Monitoring

ThermoFisher Scientific

Carlsbad (CA)

On-site

USD 90,000 - 113,000

Full time

14 days+

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Benefits offered by this job

Total Rewards package
401(k) plan
Paid time off (PTO)

Job summary

Thermo Fisher Scientific is hiring a Senior Clinical Research Associate I to monitor sites in a high-volume, client-focused environment. You will conduct remote and on-site visits, ensure protocol and regulatory adherence, manage essential documents, and support investigator payments.

This role requires strong communication, problem solving, and a deep understanding of CTMS and trial management. You will operate within our FSP model, dedicated to a single client, coordinating with clinical teams

Qualifications

  • Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
  • 3+ years experience in clinical research or equivalent.
  • Oncology experience preferred.

Responsibilities

  • Monitor investigator sites with a risk-based monitoring approach.
  • Perform remote or on-site visits to assess protocol and regulatory compliance.
  • Ensure ICH-GCP guidelines and SOPs are followed; manage documentation.
  • Coordinate investigator payments and site communications.
  • Maintain study systems and generate status/update reports.

Skills

Site monitoring
Communication
ICH-GCP knowledge
Problem solving
CTMS experience

Education

Bachelor's degree in life sciences or RN certification
3+ years clinical research experience
Oncology experience preferred

Tools

CTMS

Job description

Thermo Fisher Scientific is hiring a Senior Clinical Research Associate I to monitor sites in a high-volume, client-focused environment. You will conduct remote and on-site visits, ensure protocol and regulatory adherence, manage essential documents, and support investigator payments.

This role requires strong communication, problem solving, and a deep understanding of CTMS and trial management. You will operate within our FSP model, dedicated to a single client, coordinating with clinical teams

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