Clinical Research Associate I (CRA)

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.

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

• 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

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.