What You'll Do

Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Monitors investigator sites with a risk-based monitoring approach, applying root cause analysis and problem-solving skills to ensure compliance. Documents observations in reports and letters in a timely manner and escalates observed deficiencies to clinical management.

What We're Looking For

Bachelor's degree in a life science related field or equivalent. Considerable clinical research monitoring experience (comparable to 5+ years) with expertise in clinical monitoring. Expert knowledge of FDA guidelines, ICH GCPs, and applicable regulations.

What We Offer

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific provides outstanding career and development prospects within an innovative organization.

Additional Information

Experience Level

Senior

Job Language

English

Employment Type

Full-time

Work Mode

Remote