Clinical Research Associate

CCS-Global; Remote; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading clinical research organization is seeking a CRA II Senior / Lead Clinical Research Associate for a remote position in Germany. This role involves managing site monitoring for clinical trials, ensuring compliance with regulations, and mentoring junior CRAs. The ideal candidate will have at least 1.5 years of monitoring experience, strong GCP knowledge, and fluency in German and English. The organization values employee well-being and offers career development opportunities.

Qualifikationen

• Minimum 1.5 years of independent monitoring experience within clinical research.
• Understanding of local German regulations and ICH-GCP.
• Experience in Oncology, Haemato-oncology or Rare Diseases is desirable.

Aufgaben

• Manage all aspects of site monitoring across German study sites.
• Build relationships with Investigators and site staff.
• Ensure adherence to study protocols and regulatory requirements.
• Contribute to the development of study-related documents.
• Mentor junior CRAs for Lead level positions.

Kenntnisse

Independently managing site monitoring

Strong understanding of GCP

Excellent communication skills

Fluency in German and English

Proactive and detail-oriented approach

Jobbeschreibung

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.

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.

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.

To Apply

Please submit your CV to [e-mail]