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Senior Clinical Research Associate

AL Solutions

Düsseldorf

Vor Ort

EUR 50.000 - 70.000

Vollzeit

Vor 8 Tagen

Zusammenfassung

A leading global CRO is seeking an experienced Clinical Research Associate (CRA) in Düsseldorf, Germany. The role involves overseeing clinical trials, ensuring compliance with regulations, and building strong relationships with sites. Ideal candidates will have a Bachelor’s degree in Life Sciences or a related field, fluent German and English skills, and at least 3 years of CRA experience. The position offers competitive compensation and opportunities for career growth within the company.

Leistungen

Competitive compensation
Comprehensive benefits package
Opportunities for career growth
Flexible working arrangements
Access to innovative technology
Commitment to work-life balance

Qualifikationen

  • 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, especially Oncology or Immunology.

Aufgaben

  • Conduct site qualification, initiation, monitoring, and close-out visits across Germany.
  • Ensure compliance with ICH-GCP and German regulatory guidelines.
  • Build strong relationships with site personnel and sponsor stakeholders.

Kenntnisse

Independent monitoring experience
Fluent in German
Fluent in English
Time-management skills
Organizational skills
Communication skills

Ausbildung

Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field

Tools

CTMS
eTMF
EDC platforms

Jobbeschreibung

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.

The Role

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.

Key Responsibilities

  • 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 escalate 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 .

Requirements

  • 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 .

What’s in It for You?

  • 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 .

If you’re an ambitious CRA eager to contribute to impactful research within a supportive and high-performing team, we want to hear from you . Apply today and take the next step in your clinical research career in Germany !

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