Job Summary
We are seeking a Subject Matter Expert in Pharmacovigilance with 2 to 4 years of experience to join our team. The ideal candidate will have a strong background in Pharma Research & Development and a keen interest in PV data management and case processing. This hybrid role offers the opportunity to work in a dynamic environment contributing to the safety and efficacy of pharmaceutical products.
Responsibilities
Conduct thorough analysis of pharmacovigilance data to ensure compliance with regulatory standards and enhance drug safety.Collaborate with cross-functional teams to support the development and implementation of pharmacovigilance strategies.Provide expert guidance on PV case processing to ensure accurate and timely reporting of adverse events.Utilize technical skills in Pharma Research & Development to drive innovation and improve pharmacovigilance processes.Monitor and evaluate the effectiveness of pharmacovigilance systems and recommend improvements.Develop and maintain comprehensive documentation of pharmacovigilance activities and findings.Assist in the preparation of regulatory submissions and safety reports to ensure compliance with global standards.Engage in continuous learning to stay updated on the latest trends and advancements in pharmacovigilance.Support the training and development of team members to enhance overall team performance.Ensure data integrity and accuracy in all pharmacovigilance activities to maintain high-quality standards.Participate in audits and inspections to demonstrate compliance with regulatory requirements.Foster a culture of safety and vigilance within the organization to protect public health.Contribute to the companys mission by ensuring the safe and effective use of pharmaceutical products.
Qualifications
Possess a strong foundation in Pharma Research & Development essential for driving pharmacovigilance initiatives.Demonstrate expertise in PV data management and case processing enhancing the quality of safety assessments.Exhibit excellent analytical skills to interpret complex pharmacovigilance data and derive actionable insights.Show proficiency in regulatory compliance ensuring adherence to global pharmacovigilance standards.Display effective communication skills to collaborate with cross-functional teams and stakeholders.Maintain a proactive approach to problem-solving ensuring timely resolution of pharmacovigilance issues.
Certifications Required
Certified Pharmacovigilance Professional (CPP) or equivalent certification preferred.
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.
