Sathvika Govind

Senior Regulatory Affairs Specialist

Role
Senior Regulatory Affairs Associate at Parexel
Location
Bengaluru, KA, IN
LinkedIn followers
500 followers

About Sathvika Govind

I believe in this statement \" Never Stop Learning; For when we stop learning we stop growing \". With 4 years of experience as a Regulatory Affairs Specialist I play a pivotal role in ensuring compliance and facilitating the successful submission of regulatory documents to health authorities. My primary responsibility is to meticulously plan and execute submission strategies, adhering to stringent timelines to meet regulatory requirements. I am committed to ensuring the timely and successful submission of regulatory documents, contributing to the overall regulatory compliance.My professional experience aided me in discovering and enhancing my management and regulatory skills. I intend to emphatically concentrate on my regulatory and project management skills to develop into a global pioneer in the regulatory field.

Experience

  1. Senior Regulatory Affairs Associate

    Parexel

    Aug 2024 — Present · IN

Education

  • MS Ramaiah University of Applied Sciences

    Doctor of Pharmacy - PharmD, Clinical, Hospital, and Managed Care Pharmacy

    2012 — 2018

  • Northeastern University

    Masters of Science in Regulatory Affairs for Drugs, Biologics & Medical Devices, Pharmacy Administration and Pharmacy Policy and International Regulatory Affairs

    2019 — 2021

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Sathvika Govind — Senior Regulatory Affairs Associate at Parexel in Bengaluru, KA, IN | Unifers