Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2024) is consistently listed among the most admired companies in the world.
Post : Associate Returnship Program
Job Summary
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.
Job Description
• 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.
Candidate Profile
• 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.
Additional Information
Experience : Strong expertise in Pharma Research & Development
Location : Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Job category : Technology & Engineering
End Date : 30th September 2025
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