Clinical Research Associate II — Global Monitoring & Sites

ThermoFisher Scientific; Denmark; Remote; DKK 520,000 - 760,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) to join our global team. You will monitor investigator sites, ensure regulatory compliance, and manage essential documentation across trials, including remote and on-site activities.

You will collaborate with sponsors and sites to guarantee data integrity and patient safety. You will perform site visits, manage trials per ICH-GCP, communicate findings, and support study management with documentation and publications.

Qualifications

• Bachelor's degree in life sciences or nursing certification required.
• 1 year of clinical research monitoring experience or PPD fellowship.
• Valid driver's license where applicable.
• Equivalency may be accepted for education/experience.

Responsibilities

• Monitor investigator sites using risk-based monitoring and ensure data accuracy.
• Review SDR/SDV/CRF and maintain timely site documentation.
• Coordinate monitoring visits, communicate findings, and drive issue resolution.
• Assist in investigator meetings and site initiation activities.
• Ensure essential documents meet ICH-GCP and regulatory standards.
• Provide trial status updates and maintain study systems as required.
• Support publications/tools preparation and contribute to process improvements.

Skills

Clinical monitoring

ICH-GCP knowledge

Regulatory knowledge

Attention to detail

Communication skills

Teamwork

Microsoft Office

English proficiency

Problem solving

Education

Life sciences degree

Nursing certification

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) to join our global team. You will monitor investigator sites, ensure regulatory compliance, and manage essential documentation across trials, including remote and on-site activities.

You will collaborate with sponsors and sites to guarantee data integrity and patient safety. You will perform site visits, manage trials per ICH-GCP, communicate findings, and support study management with documentation and publications.