Kautilya Srivastava

... Functional Expertise

  • Consulting
  • Program Management

... Education

  • Babu Banarasi Das National Institute of Technology and Management,Lucknow (UPTU)

    B.Tech (Bachelor of Technology) - Information Technology

... Professional Recognitions

  • TCS- Rising Star (Account level)

  • TCS-Best Team Player (Project level)

... Extra-Curricular Activities

  • Completed Half Marathon- organised by Runizen (Noida 2018)

  • District level Archer

Kautilya Srivastava

Kautilya Srivastava

I have around 12 years of experience in Software Development and Consulting for Pharma companies. Expertise in Product Development, Agile Methodology, Requirements Management, and Stakeholder Management. Cross geographical experience with teams in Japan, EMA and US. As a Consultant, I undertook projects involving risk assessment and regulatory compliance management in the field of Pharmacovigilance.

... Work Exp | 12 years

...Associate Principal Consultant
...Prudentia Management and Technology Consulting LLP

  • Responsible for understanding client requirements, designing business solutions and providing domain consulting to the pharmaceutical companies
  • Managed relationships with multiple vendors to drive implementation, maintenance and operation of PV technology products that ensure global compliance
  • Led cross-functional teams in various implementation and maintenance projects of pharma companies.

... Senior Consultant

  • As an Account Rep, ensured proper triaging of service requests, provided weekly status updates and bill the client on quarterly basis as per the SOW
  • Mentored Consultants and clients in the Change, Risk and Deviation Management Process.
  • Provided custom solutions for complex Service Requests and enabled customers to meet the Regulatory Compliances.

... Senior Consultant

  • Created the triggers, functions and packages for safety report submissions to resolve multiple complex issues related to regulatory compliance checks.
  • Collaborated with the stakeholders to ensure regulatory timeframes are met for the reporting of patient safety information to regulatory authorities.
  • Steered the validation team of 5 consultants and developed dynamic test scripts that reduced the total turnaround time of projects by 25%.

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