Clinical Research Associate I (CRA)

Clinical Research Associate I (CRA)Full-timeCompany DescriptionPSI 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 DescriptionReady 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, GermanyYou will:Conduct and report all types of onsite monitoring visits as well as remote visitsPerform CRF review, source document verification and query resolutionMaintain accurate trial documentation, and help ensure participant safety, data integrity and compliance with study protocols and regulatory requirementsBe responsible for site communication and managementBuild effective relationships with investigators and study teamsBe involved in site identification processQualificationsCompleted 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 fieldDemonstrated knowledge and understanding of Good Clinical Practice and clinical trial processesPrior experience in clinical research is preferrableStrong communication and organizational skillsAttention to detail and willingness to take accountabilityAbility to manage several priorities and learn quicklyVery good German and English language skillsWillingness to travel to investigational sites within GermanyAdditional InformationWhy 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 patientsGrowth OpportunitiesPSI 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.By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy applyI'm interestedI'm interestedPrivacy Notice