Rafaela Mroz

Background

About Rafaela Mroz

Biomedical science graduate with a qualification in clinical analysis and a specialization in Clinical Research (Lato sensu). With 10 years of progressive experience in clinical trials (Phases I-IV), I am deeply passionate about advancing clinical research to enhance patient outcomes and improve healthcare solutions.My expertise spans Clinical Trial Assistance, Clinical Trials Coordination, and Management, particularly in Decentralized and Hybrid Clinical Trials (DCTs). I am skilled in:PharmaceuticsElectronic Data Capture (EDC)Clinical Data ManagementGood Clinical Practice (GCP)Mobile Health Visits for Clinical TrialsDecentralized Clinical Trials (DCT)I bring experience in various therapeutic areas, including oncology, hematology, nephrology, endocrinology, rheumatology, dermatology, infectology, and rare diseases.Currently, I work as Clinical Manager at mdgroup, where I lead the coordination and management of global DCT/hybrid projects. As the primary point of contact among sponsors, CROs, sites, healthcare providers, and patients, I ensure seamless communication and service delivery. Upholding ICH-GCP standards and compliance with country and local regulations. Enhancing patient recruitment, engagement, and retention rates. Delivering exceptional patient experiences to foster clinical trial excellence.Previously, I held the position of Home Health Country Coordinator – Brazil at mdgroup, where I honed my ability to balance the needs of patients and sponsors while maintaining operational excellence.With a steadfast commitment to excellence and a patient-centered approach, I strive to make a meaningful impact in the clinical research field. By fostering collaboration, innovation, and compassion, I am dedicated to advancing healthcare solutions that improve lives and set new standards for clinical trial quality and success.