Clinical Research Associate I (CRA) in Muenchen, Deutschland

PSI is a leading Contract Research Organization (CRO) with over 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

Job Description

Ready to put your theoretical knowledge into practice and take the next step in clinical research as a CRA?

At PSI CRO, we believe great CRAs can be developed, not simply hired. We are looking for a Junior Clinical Research Associate who is curious, motivated to learn, and ready to grow into clinical monitoring. You will work with experienced clinical research professionals, build hands-on knowledge of clinical trials, and develop the skills needed to manage investigative sites with confidence.

Office-based in Munich, Germany

You will:

• Conduct and report all types of onsite monitoring visits as well as remote visits
• Perform CRF review, source document verification and query resolution
• Maintain accurate trial documentation, and help ensure participant safety, data integrity and compliance with study protocols and regulatory requirements
• Be responsible for site communication and management
• Build effective relationships with investigators and study teams
• Be involved in site identification process

Qualifications

• Completed advanced CRA/Clinical Monitoring training (e.g., mibeg, Pharmaakademie, or comparable)
• University degree in life sciences, natural sciences, pharmacy, medicine, or another relevant scientific/healthcare field
• Demonstrated knowledge and understanding of Good Clinical Practice and clinical trial processes
• Prior experience in clinical research is preferrable
• Strong communication and organizational skills
• Attention to detail and willingness to take accountability
• Ability to manage several priorities and learn quickly
• Very good German and English language skills
• Willingness to travel to investigational sites within Germany

Additional Information

Why join PSI CRO?

Learn from experienced professionals. We have a strong focus on developing talent internally and providing junior professionals with the opportunity to build a long-term career in clinical research.

Build broad experience. Our CRAs can work across multiple sponsors and therapeutic areas rather than being permanently aligned to one sponsor, helping you develop a wider range of expertise.

Do work that matters. As a CRA, you contribute to the quality of clinical trials and ultimately to the development of new treatments for patients

Growth Opportunities

PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.