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Mark Ticktin
Associate Director, Clinical Data Management / Manager, Global Data Standards at Merck
Mark Ticktin is a professional with a strong passion for advancing scientific and technological ideas and aiding teams in problem-solving.
He believes in simplifying complex problems by breaking them down into manageable steps to drive progress.
Mark specializes in distilling vague concepts into clear messages, utilizing his presentation skills and technical expertise to enhance communication and foster understanding among diverse groups.
With extensive experience in GXP regulated environments, Mark has worked in various capacities ranging from in vitro laboratory settings to clinical research and data management in startups and leading pharma companies.
His academic background in Biomedical Engineering, focusing on Systems and Imaging, has fueled his interests in signal processing, research, product development, and project management.
He is particularly keen on biotech startups, specifically in medical devices and clinical science, and excels in process improvement, systems engineering, biosignals, data and project management, product management, as well as computer troubleshooting and programming.
Mark Ticktin holds a BS in Biomedical Engineering from Drexel University and has held key positions in reputable organizations like Merck, ERT, and iCardiac, showcasing expertise in clinical data management, global data standards, SAS programming, research projects, strategic implementation, operations, project management, and product development.
Throughout his career, Mark has demonstrated a knack for enhancing team performance, fostering innovation, and driving projects to successful outcomes.