Marco S. Email & Phone Number

With over a decade of experience in study coordination and project management within preclinical research, I’m passionate about driving quality and efficiency in complex study environments. My background spans the coordination of 50+ preclinical studies, ensuring timeline adherence, regulatory compliance, and strong client relations across global collaborations. I thrive in high-stakes, multi-project settings, adeptly balancing protocol development, logistical support, and client engagement to deliver impactful results.Key areas of expertise include:Preclinical Study Coordination: Skilled in managing study initiation, execution, and reporting with a consistent record of on-time completions.Regulatory Compliance & Quality Control: Proficient in ICH, GLP, FDA CFR, OECD, and Animal Welfare standards.Client & Stakeholder Relations: Dedicated to fostering positive, productive partnerships with 40+ pharmaceutical, biotech, and academic clients through transparent communication and responsive support.Data Management & Reporting: Experienced in developing, reviewing, and optimizing study reports, ensuring accuracy and reliability through statistical analysis and data integrity checks.Mentorship & Leadership: Committed to guiding teams and junior staff, promoting knowledge sharing, and ensuring project alignment.In addition to my BA in Psychology, I hold certificates in Good Clinical Practice, Good Manufacturing Practices, Medical Terminology and Microsoft Excel. My technical proficiency spans EDMS, EDCS, and the Microsoft Office Suite, empowering me to streamline workflows and maximize team productivity.I’m always open to connecting with fellow professionals, sharing insights, and exploring new opportunities where I can leverage my skills to advance impactful research.

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  Kean University

  Bachelor'S Degree