With over 9 years of experience in clinical research, I am a passionate, adaptable, and detail-oriented researcher dedicated to expanding scientific horizons and enhancing clinical outcomes. My strong attention to accuracy, combined with a logical approach and solid scientific and numerical skills, has been the foundation of my career development.I have extensive expertise in designing and validating eCRFs and am certified as a Medidata Rave study builder. My experience spans building studies on platforms such as Oracle Clinical (OC), Classic Rave, and Rave X.I have worked with a variety of electronic data capture (EDC) tools, including OC, Classic Rave, Rave X, Inform, Alea and Open Clinica. My experience includes setting up and managing complex Phase 1, 2, and 3 studies in oncology, rare diseases, and diabetes. I am skilled in protocol interpretation, SDTM annotations, preparing SAS listings, generating study metrics reports, writing data validation/edit checks, and creating test cases for validation.In addition, I bring strong project management capabilities in clinical data management, overseeing timelines, resource planning, and ensuring the successful execution of study milestones. I serve as a Subject Matter Expert (SME) for local and central lab activities, study start-up tasks, UAT activities, and data validation processes.Following my work in clinical trials and drug development, I pursued further education in the public health and nutrition sector, earning a Master of Advanced Studies (MAS) in Nutrition and Health from ETH Zurich. I am now seeking opportunities in public health and nutrition, while continuing to apply my expertise in clinical trials.Please DM me for a opportunity which aligns with my profile. Thank you!
