Germany
2 months agoJob Overview
Job Type
Full TimePay
Not disclosedJob description
- Location:
- Germany
- Work arrangement:
- On-site
Role Summary
Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As an unblinded Clinical Research As sociate , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.
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
Requirements
- 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 the Ruhrgebiet or Frankfurt region and across Germany as required
- Strong organizational skills with attention to detail
Benefits
- 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.
- Role:
- Unblinded CRA I based in Frankfurt or Ruhr Area
- Job Type:
- Full Time
Company profile
Fortrea
fortrea.comFortrea is a global contract research organization that runs Phase I to IV clinical trials for drug developers. It builds on more than 30 years of experience as Covance, which developed within Labcorp, and it provides patient-focused clinical solutions that help speed clinical development and bring new therapies to the patients who need them most.