Archives: Speakers

With nearly 20 years of experience in clinical research, she has developed extensive expertise in biostatistics, clinical data management, EDC systems, database development, SAS programming, and CDISC standards (SDTM and ADaM).
She is a Medidata Rave Certified Builder and possesses comprehensive experience in clinical database design, EDC implementation, and end-to-end clinical trial data management. Throughout her career, she has supported a wide range of Phase I-IV clinical studies across multiple therapeutic areas and has developed a strong understanding of clinical trial workflows, regulatory requirements, and sponsor expectations.
In addition, she has contributed to numerous regulatory submission programs, supporting successful marketing applications and approvals by the FDA, EMA, and Health Canada. Her experience spans statistical programming, clinical data standards, submission-ready datasets, and cross-functional collaboration to ensure high-quality and compliant clinical trial deliverables.
In her current role, she focuses on understanding client needs, building strategic partnerships, and identifying innovative opportunities to improve clinical trial efficiency and data quality.

Murali is Director of Business Development at Pharmsky Research, with 19+ years in manufacturing and supply chain across pharma, biotech and medical devices. He has held roles at Roche, Genentech, Novartis, Menarini, Cardinal Health and most recently at Cerecin, a global biotech, where he was Senior Director of Manufacturing & Supply. He holds a Master’s Degree in Chemical Engineering from the National University of Singapore and a MBA from the University of Strathclyde, Glasglow

Michael Pröschel is responsible for overall commercial and operational management and strategic process optimization. He has over 25 years of experience in the life science industry (clinical research, pharmaceutical industry and digital health technologies), both in national and international functions.