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
Acerca de Cognizant
Cognizant (Nasdaq: CTSH) es un creador de soluciones de IA y proveedor de servicios tecnológicos que conecta la inversión en IA con el valor empresarial mediante el desarrollo de soluciones de IA full‑stack para sus clientes. Su profundo conocimiento de la industria, junto con su experiencia en procesos e ingeniería, permite incorporar el contexto único de cada organización en sistemas tecnológicos que amplifican el potencial humano, generan resultados tangibles y mantienen a las empresas a la vanguardia en un entorno en constante cambio. Más información en cognizant.ai o @cognizant.
Información adicional de empleo
La información de compensación es precisa a la fecha de esta publicación. Cognizant se reserva el derecho de modificar esta información en cualquier momento, sujeto a la legislación aplicable.
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Cognizant es un empleador que ofrece igualdad de oportunidades. Tu solicitud y candidatura no serán consideradas en base a raza, color, sexo, religión, credo, orientación sexual, identidad de género, origen nacional, discapacidad, información genética, embarazo, condición de veterano o cualquier otra característica protegida por las leyes federales, estatales o locales.
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