Job Summary
Join our team as a Specialist in Pharmacovigilance where you will leverage your expertise in Pharma Research & Development to ensure the safety and efficacy of pharmaceutical products. With a focus on PV data management and case processing you will play a crucial role in monitoring and evaluating drug safety. This hybrid role offers a dynamic work environment with no travel required allowing you to contribute effectively during day shifts.
Responsibilities
- Monitor and evaluate drug safety data to ensure compliance with regulatory standards and company policies.
- Collaborate with cross-functional teams to analyze and interpret pharmacovigilance data for accurate reporting.
- Develop and implement strategies to enhance the efficiency of PV case processing and data management.
- Provide insights and recommendations based on data analysis to improve product safety and efficacy.
- Ensure timely and accurate documentation of adverse event reports and safety assessments.
- Assist in the preparation of regulatory submissions and safety reports to support product approvals.
- Conduct regular audits of PV processes to identify areas for improvement and ensure quality control.
- Facilitate training sessions for team members to enhance their understanding of pharmacovigilance practices.
- Utilize advanced tools and methodologies to streamline data collection and analysis processes.
- Coordinate with global teams to ensure consistency in pharmacovigilance operations and reporting.
- Support the development of risk management plans and safety monitoring strategies.
- Engage in continuous learning to stay updated with the latest industry trends and regulatory changes.
- Contribute to the companys mission of ensuring public health and safety through diligent pharmacovigilance practices. Qualifications
- Possess a strong background in Pharma Research & Development with hands-on experience in pharmacovigilance.
- Demonstrate expertise in PV data management and case processing showcasing a keen eye for detail.
- Exhibit excellent analytical skills to interpret complex data and provide actionable insights.
- Have a proactive approach to identifying and resolving issues related to drug safety.
- Show proficiency in using pharmacovigilance software and tools for efficient data handling.
- Display strong communication skills to collaborate effectively with cross-functional teams.
- Maintain a commitment to continuous learning and professional development in the field of pharmacovigilance.
Certifications Required
Certified Pharmacovigilance Professional (CPP) Advanced Pharmacovigilance Certification
About Cognizant:
Cognizant (Nasdaq: CTSH) is an AI Builder and technology services provider, bridging the gap between AI investment and enterprise value by building full-stack AI solutions for our clients. Our deep industry, process and engineering expertise enables us to build an organization’s unique context into technology systems that amplify human potential, drive tangible outcomes and keep global enterprises ahead in a fast-changing world. See how at cognizant.ai or @cognizant.
Additional employment information
Compensation information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.
Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.
Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
