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Data AnalysisCompliance

1 month ago

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Important information


Contract type:

Permanent

Location:

Pune, Maharashtra, India

Work mode:

Onsite

Published on:

21 September 2026

What they need


Job Summary

We are seeking an experienced professional for the role of TL-Pharmacovigilance with 6 to 9 years of experience. The ideal candidate will have expertise in Pharma Research & Development and proficiency in MS Excel. Experience in PV Case Processing and Pharmacovigilance & Safety Ops is a plus. The role involves a hybrid work model with rotational shifts.

Responsibilities

  • Oversee the pharmacovigilance activities to ensure compliance with regulatory requirements and company standards.
  • Provide expertise in Pharma Research & Development to enhance the quality and efficiency of safety operations.
  • Utilize MS Excel to analyze and report pharmacovigilance data accurately and efficiently.
  • Coordinate with cross-functional teams to ensure seamless integration of safety data into the overall drug development process.
  • Monitor and evaluate adverse event reports to identify potential safety signals and trends.
  • Ensure timely and accurate case processing in accordance with standard operating procedures.
  • Collaborate with global teams to harmonize pharmacovigilance practices and share best practices.
  • Develop and implement safety monitoring plans to proactively manage potential risks.
  • Conduct regular audits and assessments to ensure compliance with pharmacovigilance regulations.
  • Provide training and guidance to junior staff on pharmacovigilance processes and procedures.
  • Support the preparation of safety reports and regulatory submissions.
  • Engage in continuous improvement initiatives to enhance pharmacovigilance operations.
  • Maintain up-to-date knowledge of pharmacovigilance regulations and industry trends.

Qualifications

  • Demonstrate strong expertise in Pharma Research & Development with a focus on safety operations.
  • Exhibit proficiency in MS Excel for data analysis and reporting.
  • Possess experience in PV Case Processing and Pharmacovigilance & Safety Ops as a valuable asset.
  • Show ability to work effectively in a hybrid work model with rotational shifts.
  • Display excellent communication and collaboration skills to work with cross-functional teams.
  • Have a keen eye for detail and a proactive approach to identifying and managing risks.

Certifications Required

Certified Pharmacovigilance Professional (CPP) or equivalent certification preferred.

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