Unblinded CRA I/II — Global Trials & Flexible Work

Fortrea; Wien; Hybride; EUR 48 000 - 64 000; Plein temps

Avantages offerts par ce poste

Structured onboarding

Flexible working model

Global career growth

Inclusive culture

Wellbeing initiatives

Résumé du poste

Fortrea in Austria is seeking an unblinded Clinical Research Associate (CRA I or CRA II) to support unblinded study activities within a sponsor-dedicated environment. You will contribute to high-quality clinical research delivery while gaining exposure to unblinded processes in a collaborative global setting.

The role offers structured onboarding, flexible working arrangements, and opportunities for professional growth in clinical operations across the DACH region, with travel within

Qualifications

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

Responsabilités

• Perform unblinded monitoring in line with ICH-GCP and regulations.
• Ensure protocol compliance, data integrity, and patient safety at sites.
• Maintain study documents, eTMF, and regulatory files.
• Engage site staff as primary contact for site management (pharmacy only).
• Contribute to audit readiness and inspections at site level.

Connaissances

Unblinded monitoring

ICH-GCP knowledge

German language

English language

Travel willingness

Attention to detail

Organizational skills

Formation

Bachelor’s degree in Life Sciences or related field

Description du poste

Fortrea in Austria is seeking an unblinded Clinical Research Associate (CRA I or CRA II) to support unblinded study activities within a sponsor-dedicated environment. You will contribute to high-quality clinical research delivery while gaining exposure to unblinded processes in a collaborative global setting.

The role offers structured onboarding, flexible working arrangements, and opportunities for professional growth in clinical operations across the DACH region, with travel within