Tanzeel Ur Rehman

WORK HISTORY

EDUCATION

SKILLS

ABOUT TANZEEL UR REHMAN

I am a Ph.D-trained scientist and Clinical Project Manager with a strong interdisciplinary background in bioanalytical study management, biomaterials, and pharmaceutical R&D. At Worldwide Clinical Trials, I manage clinical and bioanalytical studies from initiation to final reporting, serving as the key liaison between sponsors and laboratory teams. My role bridges science and operations—ensuring regulatory compliance (GLP, GCP, FDA 21 CFR Part 11), efficient project execution, risk mitigation, and on-time data delivery.With over a year at Worldwide, I’ve contributed to the design, tracking, and oversight of complex studies, applying both technical acumen and project management skills. I’ve led initiatives to improve visibility across teams using tools like Power BI, Watson LIMS, and Trackwise, and supported inspection readiness across projects.Previously at Nulixir Inc, I developed next-gen nanoparticle-based delivery systems for functional beverages—encapsulating bioactives like Vitamin D3 and Omega-3 using liposomes and emulsion techniques. This work strengthened my expertise in GMP-regulated R&D, analytical characterization (LC-MS/MS, HPLC, DLS, FTIR), and client-focused innovation.Throughout my career, I’ve built a reputation for scientific rigor, cross-functional collaboration, and process-driven problem solving. Whether managing timelines and budgets or translating data into regulatory deliverables, I bring clarity, ownership, and precision to everything I do.I’m passionate about driving clinical progress and improving global health outcomes through effective study execution, regulatory integrity, and materials-driven innovation.Let’s connect if you’re interested in clinical operations, project leadership, or advancing science through smarter systems and solutions.