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.
关于高知特 (Cognizant)
高知特(Cognizant)（纳斯达克代码：CTSH）作为一家AI Builder和相关技术服务提供商，致力于通过打造全栈AI解决方案，帮助企业将人工智能投资转化为实际价值。公司凭借深厚的行业经验、流程优化和工程技术专长，将企业独特的业务场景融入科技系统，赋能组织释放人才潜能，推动切实成果，并帮助全球企业在瞬息万变的环境中保持领先。如需了解更多详情，敬请访问 cognizant.ai 或关注@cognizant。
补充雇佣信息
薪酬信息截至本职位发布之日为准。Cognizant 保留在适用法律允许的范围内随时修改该信息的权利。
申请人可能需要通过现场面试或视频会议的方式参加面试。此外，候选人在每次面试时可能需要出示其当前所在州或政府签发的有效身份证件。
Cognizant 是一家提供平等就业机会的雇主。在招聘过程中，您的申请和候选资格不会因种族、肤色、性别、宗教、信仰、性取向、性别认同、国籍、残疾、遗传信息、怀孕、退伍军人身份或任何其他受联邦、州或地方法律保护的特征而受到影响。
