CRA II / Senior Clinical Research Associate - Germany

Are you an experienced CRA looking for your next significant career step within the German clinical landscape? Do you thrive in an environment that values a thoughtful approach to site management and prioritises employee well-being? If so, we have a great opportunity for you to join our leading team in

Germany . If you have a minimum of 1.5 years as a monitor, then please get in touch...

Our client, a global CRO, is seeking a highly motivated

CRA II, Senior or Lead CRA

to contribute to the advancement of ground-breaking therapies across a range of compelling areas, including Oncology, Haemato-oncology, Rare Diseases, and other innovative fields. You will play a crucial role in ensuring the smooth and efficient conduct of clinical trials, working with a network of sites across Germany.

What sets this team apart? Focus on Quality, Not Just Metrics:

They champion a solid thought process in site management, understanding that effective collaboration and proactive problem-solving are paramount. The team empowers their CRAs to manage their sites effectively without the burden of a rigid "minimum days on site" quota. Genuine Career Development:

The organisation is deeply invested in the growth of its team members. You can expect clear pathways for career progression, supported by ongoing training and mentorship opportunities tailored to the German market and global standards. Exceptional Team Retention:

By fostering a supportive and engaging work environment where individuals feel valued, this team enjoys high retention rates. Their commitment to clear communication and work-life balance translates into a truly collaborative spirit. Meaningful Employee Engagement:

Your insights will help shape integral processes and contribute to a positive workplace. This focus on engagement is a cornerstone of their long-term success and the longevity of their team members' careers.

Key Responsibilities: Independently managing all aspects of site monitoring, from initiation to close-out, across German study sites. Building and maintaining strong relationships with Investigators and site staff (SNCs). Ensuring strict adherence to study protocols,

ICH-GCP , and local German regulatory requirements ( AMG/StrSchV ). Contributing to the development of study-related documents. Mentoring and supporting junior CRAs (for Lead level positions).

Your Profile: Significant independent monitoring experience within clinical research, specifically within the German healthcare system. A strong understanding of GCP and relevant local regulations. Fluency in German and English

(both written and spoken) is essential. Excellent communication, organisation, and problem-solving skills. A proactive and detail-oriented approach. Experience in Oncology, Haemato-oncology, or Rare Diseases is highly desirable. Part-time (4 days per week) will be considered

If you are looking for a rewarding career where your expertise is valued, your professional development is prioritised, and you can contribute to the advancement of truly innovative medicines, we encourage you to apply.

Please note - all applicants MUST be 100% fluent in spoken and written German

To Apply:

For a confidential discussion please call Andy Smith on +44 (0) . Alternatively please submit your CV to