Oncology-Focused Clinical Research Associate (Finland)

FTFIN Fortrea Development Ltd Suomen sivuliike; Helsinki; On-site; EUR 55,000 - 75,000; Full time

Job summary

Fortrea Finland is seeking a Clinical Research Associate (CRA) to monitor oncology studies and sponsor-dedicated trials in southern Finland. The role involves site management, regulatory documentation, source data verification, and ensuring patient safety and data integrity through ICH-GCP guidelines.

Travel is required; you will conduct pre-study, initiation, monitoring, and close-out visits, with training and collaboration across a study team.

Qualifications

• University or college degree in a related allied health field; nursing licensure preferred.
• Fluent in English; local language plus English required.
• Strong understanding of ICH GCP guidelines and local regulatory requirements.

Responsibilities

• Manage clinical studies at the site level following SOPs, ICH GCP, and sponsor requirements.
• Perform site monitoring visits: Pre-study, Initiation, Monitoring, Close-out; ensure data integrity and subject protection.
• Verify regulatory documents, ensure IP accountability, and prepare trip reports.

Skills

English language

GCP knowledge

Site monitoring

Education

University degree in nursing or allied health

Tools

eClinical systems

Job description

Fortrea Finland is seeking a Clinical Research Associate (CRA) to monitor oncology studies and sponsor-dedicated trials in southern Finland. The role involves site management, regulatory documentation, source data verification, and ensuring patient safety and data integrity through ICH-GCP guidelines.

Travel is required; you will conduct pre-study, initiation, monitoring, and close-out visits, with training and collaboration across a study team.