Unblinded CRA in Germany or in Austria

Fortrea; Wien; Hybrid; EUR 45.000 - 65.000; Vollzeit

Benefits dieser Stelle

Sponsor-supported

Onboarding program

Flexible schedule

Global career growth

Inclusive culture

Zusammenfassung

Fortrea in Austria is seeking an unblinded Clinical Research Associate to support cutting-edge trials in the DACH region. You will perform unblinded monitoring in line with ICH-GCP and maintain site oversight and data integrity.

This role offers sponsorship-dedicated environment, structured onboarding, and flexible work models. Travel to sites in Germany and Austria, collaboration with global teams, and opportunities to advance in clinical operations.

Qualifikationen

• Bachelor’s degree in Life Sciences or related field (or equivalent experience).
• Initial experience in clinical research as a CRA with at least 1 year of monitoring experience.
• Understanding of ICH-GCP guidelines and clinical trial processes.
• Strong interest and knowledge in unblinded study conduct and Investigational Product management.
• Fluency in German and English (written and spoken).
• Willingness to travel within Germany and Austria as required.
• Strong organizational skills with attention to detail.

Aufgaben

• You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
• You will ensure protocol compliance, data integrity, and patient safety at assigned sites
• You will maintain accurate and complete study documentation, including eTMF and regulatory files
• You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
• You could contribute to audit readiness and ensure inspection preparedness at site level

Kenntnisse

ICH-GCP knowledge

German and English

Monitoring experience

Detail-oriented

Travel willingness

Ausbildung

Bachelor’s degree in Life Sciences or related field

Jobbeschreibung

Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate, you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.

Key Responsibilities

• You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
• You will ensure protocol compliance, data integrity, and patient safety at assigned sites
• You will maintain accurate and complete study documentation, including eTMF and regulatory files
• You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
• You could contribute to audit readiness and ensure inspection preparedness at site level

Required Qualifications

• Bachelor’s degree in Life Sciences or related field (or equivalent experience)
• Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
• Understanding of ICH-GCP guidelines and clinical trial processes
• Strong interest and knowledge in unblinded study conduct and Investigational Product management
• Fluency in German and English (written and spoken)
• Willingness to travel within Germany and Austria as required
• Strong organizational skills with attention to detail

What We Offer

• Opportunity to work in a sponsor-dedicated environment on innovative studies
• Structured onboarding and continuous development programs
• Flexible working model supporting work-life balance
• Access to global career growth opportunities within clinical operations
• Inclusive and collaborative culture with employee resource groups and wellbeing initiatives

If you are looking to build your clinical monitoring career within a high-impact and supportive environment, we encourage you to apply and grow with us.

Learn more about our EEO & Accommodations request here.