Germany
2 months ago

Job Overview

Job Type
Full Time
Pay
Not disclosed

Job 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 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.

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