Rodrigo Acevedo is the Director of Study Start-up Biopharma at Emmes, where they leverage extensive expertise in biopharmaceutical and CRO operations. With a strong background in start-up, site activation, and regulatory affairs across Latin America, Rodrigo has been instrumental in expanding clinical operations and driving strategy within the industry. They hold an MBA and a Diploma in Clinical Research, alongside a Bachelor of Science in Marine Biology, reflecting a solid educational foundation supporting their leadership in various roles throughout their career. Previous positions include Regulatory Director at VaxTrials and Director of Regulatory Affairs at Worldwide Clinical Trials.
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