Budapest, Budapest, Hungary
I’m a PhD Candidate in Pharmaceutical Sciences at Semmelweis University and a Research Fellow at the HUN-REN Institute of Experimental Medicine (KOKI), with over a decade of experience bridging healthcare, academia, and clinical research. My mission? To make clinical trials more inclusive, evidence-based, and patient-centered. Currently, I lead advanced research on neuropathic pain and NMDA receptor crosstalk, coordinating multidisciplinary teams using Agile/Kanban principles to ensure ethical, rigorous, and audit-ready project execution. My background spans: Clinical Research & Monitoring: Expertise in site management, Source Data Verification (SDV), and navigating the EU Clinical Trials Information System (CTIS). Hospital-Based Clinical Pharmacy: 5+ years of Investigational Product (IP) accountability and safety monitoring in tertiary care. Cross-Border Collaboration: Leading research programs across Europe and the Middle East, ensuring alignment with ICH-GCP E6 (R2) and OGYÉI standards. Scientific Impact: Published author in high-impact journals (IJMS, Pharmaceutics) and speaker at international conferences (HUPHAR, MedPécs). Core Competencies: Clinical Project Management: SQV, SIV, and IMV workflows for Phase I–III studies. Regulatory Navigation: Deep knowledge of EU Regulation 536/2014 and FDA compliance. Data Integrity: Proficiency in EDC systems (Veeva, Medidata Rave) and eTMF reconciliation. Multicultural Leadership: Facilitating diverse teams in high-pressure research environments. I’m passionate about bringing diversity, innovation, and empathy into every phase of drug development. Let’s Connect: I am always open to collaboration, co-authorship, and cross-institutional research—especially in Oncology, Neuroscience, and Rare Diseases. Whether you want to talk about the future of health equity, clinical trial optimization... or just share a great cup of Iraqi Tea with some cookies, I’d love to hear from you. #Pharmacology #ClinicalResearch #CRA #DrugDevelopment #PhDLife #HealthEquity
• Leading experimental protocols in high-tier neuropharmacological research, focusing on NMDA receptor-mediated transmission and translational pain models. • Managing sophisticated laboratory data integrity, ensuring all records meet international standards for scientific validity and peer-reviewed publication. • Collaborating with cross-functional specialist teams to accelerate therapeutic discovery in CNS disorders, aligning with EU-level research compliance frameworks.
Research Focus: Neuropathic pain, opioid tolerance, GlyT-1 inhibitors, α2-adrenergic pathways 📍 Department of Pharmacodynamics Key Contributions: Designed and conducted in vivo experiments using rat models for neuropathic pain and morphine tolerance Led cross-functional project teams using Agile frameworks to coordinate lab operations and data analysis Authored and co-authored 9+ scientific publications in peer-reviewed journals, including IJMS and Pharmaceuticals Presented original research at international conferences including HUPHAR 2024, MedPécs 2024, and PhD Scientific Days Integrated ethical standards, regulatory requirements, and data protection protocols in all research activities Mentored junior researchers and facilitated collaborative grant applications Tools & Skills: SPSS | PowerPoint | Animal handling & anesthesia | Data interpretation | Team facilitation | Publication strategy | Electrophysiology (ERG, EMG)
Academic Focus: Clinical pharmacy, research methodology, drug safety, pharmacotherapeutics Key Contributions: Delivered undergraduate and postgraduate lectures on clinical pharmacy, therapeutics, and pharmacovigilance Supervised multiple PharmD and Master's theses in clinical and pharmaceutical research Led national and international collaborative studies on medication safety, public health, and drug efficacy Spearheaded curriculum development for updated clinical training programs based on international best practices Participated in teaching and research initiatives with EU-based institutions and Middle Eastern partners Actively contributed to student development through mentoring, skills workshops, and exam board participation
Role Summary: Oversaw clinical pharmacy operations in a tertiary care hospital, integrating academic expertise into direct patient care. Key Contributions: Delivered pharmaceutical care across multiple departments, ensuring safe and effective medication use Trained, mentored, and evaluated junior pharmacists and pharmacy interns in clinical best practices Collaborated with physicians to optimize therapeutic regimens and reduce medication-related complications Implemented compliance and safety protocols aligned with hospital standards and Iraq MoHE guidelines Led initiatives to evaluate and improve pharmacy workflows, documentation, and medication reconciliation processes Spearheaded interdepartmental communication to support seamless patient transitions and continuity of care.
Focus: Experimental pharmacology, drug testing, and hypothesis-driven research Key Contributions: Designed and executed laboratory experiments on drug efficacy, pharmacokinetics, and pharmacodynamics Developed and tested hypotheses related to CNS and cardiovascular drug interactions using in vitro and in vivo models Conducted statistical analysis and interpreted pharmacological data using specialized software Authored detailed research reports and collaborated on scientific publications Managed lab equipment, safety protocols, and trained junior lab staff and research assistants Attended regional conferences to present findings and engage with the broader pharmacological research community.