Misela Duka

Background

About Misela Duka

Dedicated Clinical Research Associate (CRA II) with extensive experience in on-site and remote monitoring across multiple therapeutic areas, including oncology, neurology, hematology, rare diseases, endocrinology, ophthalmology, pulmonology, dermatology, pediatric vaccines, infectious diseases, and rheumatoid arthritis. Skilled in medical device monitoring and ensuring compliance with Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements across diverse study sites in Latvia, Lithuania, Estonia, Germany, and Switzerland. Proficient in conducting pre-study, initiation, monitoring, and close-out visits, ensuring protocol adherence and data integrity. Adept at working with Electronic Data Capture (EDC) systems, including Inform, Siebel, ICOTrial, RealTime, Complion, Florence, CRIO, eConsent, iView2, TrialManager, pTMF, SIP, VCT, ICOMaster, Activate, Fountayn, Veeva Vault, Firecrest, Sirius, IWRS, eDiary, PSO, iSPRINT, and Zelta. Strong technical skills in Microsoft Office, Oracle Clinical, genetic programs, and iMEDIDATA RAVE. Fluent in Latvian (native), English, and Russian (full professional proficiency), with B2-level working proficiency in German. Highly skilled in communication, problem-solving, and stakeholder collaboration, ensuring smooth trial execution and effective resolution of challenges. Passionate about advancing clinical research and contributing to high-quality, patient-centered trials.