Associate Returnship Program

Cognizant; Maharashtra; Hybrid; INR 1,200,000 - 1,800,000; Full time

Job summary

Cognizant is seeking an experienced TL-Pharmacovigilance with 6 to 9 years of hands-on safety operations experience to lead PV activities in a hybrid work environment. The role requires regulatory awareness and a proactive approach to risk management across global teams.

You will leverage Pharma R&D expertise, use MS Excel for data analysis and reporting, oversee PV case processing, monitor safety signals, and drive continuous improvements in safety operations and regulatory submissions.

Qualifications

• Pharma R&D safety operations expertise.
• Proficient in MS Excel for data analysis.
• Experience in PV case processing and safety operations.

Responsibilities

• Oversee pharmacovigilance activities ensuring regulatory compliance.
• Utilize MS Excel to analyze and report safety data.
• Coordinate with cross-functional teams to integrate safety data into drug development.
• Monitor adverse event reports to identify safety signals.
• Ensure timely case processing according to SOPs.
• Collaborate with global teams to harmonize PV practices.
• Provide training to junior staff on PV processes.
• Support safety reports and regulatory submissions.

Skills

Pharma safety operations

Hybrid work experience

Regulatory compliance awareness

Tools

MS Excel

Job description

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.