Senior Clinical Research Associate

Chloe O'Shea is proud to partner with a leading global CRO delivering cutting-edge solutions in clinical development. We are seeking an experienced Clinical Research Associate (CRA) to join a dynamic and dedicated team in Germany for an exciting single-sponsor opportunity. This position offers a sustainable workload of 6–8 site visits per month
, allowing you to focus on high-quality monitoring and meaningful site engagement.

As a Clinical Research Associate (CRA), you will play a critical role in overseeing the execution of clinical trials across Germany
. Collaborating closely with investigative sites and sponsor teams, you will ensure compliance with study protocols,
ICH-GCP standards
, and German regulatory requirements
. This is an ideal opportunity for professionals passionate about advancing global research within a supportive, innovation-driven environment.

• Conduct site qualification, initiation, monitoring
  , and close-out visits across Germany.
• Ensure clinical trial sites operate in compliance with ICH-GCP
  , German regulatory guidelines (e.g. AMG, GCP-V), and sponsor protocols.
• Verify source data
  , oversee investigational product accountability
  , and ensure completeness of site documentation
  .
• Identify and escalat e site-level issues proactively to support timely resolution and continuous study progress.
• Build strong, collaborative relationships with site personnel and sponsor stakeholders
  .
• Provide training and support to site staff to ensure protocol adherence and data accuracy.
• Maintain up-to-date documentation and manage clinical systems including CTMS
  , eTMF
  , and EDC platforms
  .

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy
  , or a related field.
• Minimum of 3 years of independent monitoring experience as a CRA in Germany
  .
• In-depth knowledge of ICH-GCP and the German clinical regulatory landscape
  .
• Experience across multiple therapeutic areas
  , with preference for Oncology or Immunology studies.
• Fluent in German and English
  , both written and spoken.
• Excellent organizational, communication
  , and time-management skills
  .

• Competitive compensation and a comprehensive benefits package
  .
• Opportunities for career growth within a global leader in clinical research.
• Flexible working arrangements with manageable travel expectations.
• Access to innovative technology platforms and global study networks
  .
• Commitment to work-life balance
  , mental well-being
  , and ongoing professional development
  .