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.