Smit Patel

Clinical Research Professional | ICH-GCP, FDA, EMA Compliance | Clinical Data & Trial Management | Drug Regulatory Affairs

Role
Clinical Research Associate at Cliantha Research Limited
Location
Jersey City, NJ, US
LinkedIn followers
500 followers
Healthcare & Human ServicesView LinkedIn profile

About Smit Patel

I am a Clinical Research Associate with 3+ years of experience in Phase global trials across oncology, metabolic, and multi-therapeutic areas. Skilled in ICH-GCP compliance, risk-based monitoring, and regulatory submissions, I have successfully managed 25+ trial sites with 97%+ SDV accuracy and zero audit findings. With, a Master’s in Drug Regulatory Affairs at Long Island University, I bring a strong combination of hands-on clinical monitoring expertise and growing regulatory knowledge. I am passionate about ensuring data integrity, advancing drug development, and contributing to innovative therapies that improve patient outcomes.

Experience

  1. Clinical Research Associate

    Cliantha Research Limited

    Mar 2026 — Present · US

Education

  • Long Island University

    Master of Science - MS, Drug regulatory affairs

  • L.M. College Of Pharmacy

    M.PHARM , Pharmacology

    2019 — 2021

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Smit Patel — Clinical Research Associate at Cliantha Research Limited in Jersey City, NJ, US | Unifers