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Clinical Research Associate
Job summary
A leading CRO in Germany seeks a CRA II Senior/Lead Clinical Research Associate to independently manage site monitoring. This role emphasizes quality over strict metrics, offering strong career development and mentorship. Candidates should exhibit significant independent monitoring experience within the German healthcare system, fluency in German and English, and a detail-oriented approach. This position allows contribution to innovative therapies in a collaborative and supportive environment.
Qualifications
- At least 1.5 years of independent monitoring experience in clinical research.
- Understanding of ICH-GCP, AMG, StrSchV, and local German regulations.
- Experience in Oncology, Haemato-oncology, or Rare Diseases is a plus.
Responsibilities
- Independently manage all aspects of site monitoring across German study sites.
- Build and maintain relationships with Investigators and site staff.
- Ensure adherence to study protocols and local regulations.
- Contribute to development of study-related documents.
- Mentor junior CRAs if in Lead position.
Skills
CRA II Senior / Lead Clinical Research Associate (CRA) – Remote, 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.
- 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.
- 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).
- 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.
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 submit your CV to r.kelly@completeclinicalsolutions.com
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.