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Cognizant
Join Cognizant’s Associate Returnship Program as a Team Lead – Pharmacovigilance
Cognizant is inviting experienced professionals to apply for the position of Team Lead (TL) – Pharmacovigilance under its Associate Returnship Program. This opportunity is ideal for candidates with a strong background in pharmaceutical safety operations and drug safety management who are looking to advance their careers in a dynamic, global environment.
Job Details
- Job Title: Team Lead – Pharmacovigilance
- Job ID: 00065360871
- Location: Pune, India
- Category: Technology & Engineering
- Work Model: Hybrid
- Experience Required: 6–9 Years
- Shift: Rotational Shifts
Role Overview
As a Team Lead in Pharmacovigilance, you will play a critical role in ensuring patient safety and regulatory compliance throughout the drug development lifecycle. The position requires expertise in pharmacovigilance operations, safety data management, and pharmaceutical research and development.
The successful candidate will oversee safety monitoring activities, support regulatory reporting requirements, and collaborate with global teams to enhance pharmacovigilance processes and operational excellence.
Key Responsibilities
Pharmacovigilance Leadership
- Manage pharmacovigilance activities in compliance with regulatory guidelines and organizational standards.
- Lead safety operations initiatives to ensure high-quality case processing and reporting.
- Monitor adverse event reports and identify emerging safety signals and trends.
Safety Data Management
- Utilize MS Excel and analytical tools to evaluate and report pharmacovigilance data.
- Ensure accurate and timely processing of safety cases according to established procedures.
- Support the preparation of safety reports, aggregate reports, and regulatory submissions.
Cross-Functional Collaboration
- Partner with research, development, and global safety teams to integrate safety data into drug development programs.
- Promote harmonized pharmacovigilance practices across global operations.
- Share best practices and contribute to process optimization initiatives.
Compliance & Continuous Improvement
- Conduct audits and quality assessments to maintain regulatory compliance.
- Develop and implement safety monitoring plans to proactively manage risks.
- Drive continuous improvement projects to enhance efficiency and operational effectiveness.
- Stay current with evolving pharmacovigilance regulations and industry trends.
Required Qualifications
Candidates should possess:
- 6–9 years of experience in Pharmacovigilance or Drug Safety.
- Strong expertise in Pharma Research & Development.
- Advanced proficiency in MS Excel for data analysis and reporting.
- Experience in Pharmacovigilance & Safety Operations.
- Knowledge of PV Case Processing processes and regulatory requirements.
- Excellent communication, leadership, and stakeholder management skills.
- Ability to work in a hybrid environment and rotational shifts.
- Strong analytical mindset with attention to detail and risk management capabilities.
Preferred Certification
- Certified Pharmacovigilance Professional (CPP) or an equivalent industry-recognized certification.
Why Join Cognizant?
Cognizant offers professionals an opportunity to work with global pharmaceutical clients, leverage cutting-edge technologies, and contribute to improving patient safety worldwide. Through its Associate Returnship Program, the organization supports experienced professionals in re-entering or advancing their careers while working in an inclusive and collaborative environment.
Who Should Apply?
This role is best suited for experienced pharmacovigilance professionals who have a strong understanding of safety operations, regulatory compliance, and drug safety case management, and who are looking to take on leadership responsibilities in a global healthcare environment.
APPLY HERE
Apply now and become part of Cognizant’s mission to transform healthcare through innovation, safety, and operational excellence.
To apply for this job please visit careers.cognizant.com.
