**Job Summary** Join our dynamic team as a Pharmacovigilance Associate where you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With a focus on Pharma Research & Development you will contribute to the monitoring and evaluation of drug safety data. This hybrid role offers the flexibility of rotational shifts providing a comprehensive experience in the field. **Responsibilities** + Monitor and evaluate adverse event data to ensure drug safety and compliance with regulatory standards. + Collaborate with cross-functional teams to support the development and implementation of safety monitoring plans. + Assist in the preparation and submission of safety reports to regulatory authorities. + Conduct thorough research and analysis of safety data to identify potential risks and trends. + Support the development of risk management strategies to mitigate identified risks. + Participate in the review and assessment of safety information from clinical trials and post-marketing sources. + Provide input and support for the development of safety-related documents and reports. + Maintain accurate and up-to-date records of safety data and case processing activities. + Ensure compliance with standard operating procedures and regulatory requirements. + Contribute to the continuous improvement of pharmacovigilance processes and systems. + Collaborate with team members to ensure timely and accurate case processing. + Engage in ongoing training and development to stay current with industry best practices. + Support the implementation of new pharmacovigilance tools and technologies. Qualifications + Possess a degree in a relevant scientific field such as pharmacy or life sciences. + Demonstrate strong analytical and problem-solving skills with attention to detail. + Exhibit excellent communication and interpersonal skills for effective collaboration. + Show proficiency in using pharmacovigilance databases and software. + Have a basic understanding of regulatory requirements and guidelines. + Display a keen interest in drug safety and pharmacovigilance practices. + Experience in PV Case Processing is a plus. Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.