Job Summary
Contribute to global medicine safety as a specialist in pharmacovigilance focusing on high quality pharmaceutical research and development activities for an international organization. Apply foundational experience in safety data handling and clinical documentation to support compliant case management and timely reporting. Work in a hybrid day shift model collaborating with cross functional teams to protect patient wellbeing and strengthen public trust in healthcare innovations.
Responsibilities
Perform end to end pharmacovigilance case handling activities for assigned safety reports ensuring accurate data capture narrative clarity and consistent application of internal procedures to support reliable patient safety decisions.Review source documents and clinical data from pharmaceutical research and development activities validate medical information and identify relevant safety details that contribute to robust evaluation of product risk and benefit profiles.Execute standardized workflows for spontaneous and solicited adverse event intake classification and data entry maintaining high levels of data quality and compliance with global pharmacovigilance regulations and company governance.Conduct detailed medical assessment of individual case safety reports within scope of experience confirm event seriousness and expectedness and escalate complex or medically sensitive cases to senior safety reviewers as needed.Prepare regulatory compliant individual case safety report outputs including medically coherent narratives and structured data elements to enable timely electronic submission to health authorities and business partners.Support the maintenance of case processing metrics by monitoring workload queues prioritizing urgent regulatory timelines and collaborating with colleagues so that safety reports are completed within agreed service levels.Apply knowledge of pharmaceutical research and development processes to contextualize reported adverse events recognize clinically relevant product information and contribute to accurate interpretation of safety signals.Coordinate with cross functional teams in clinical operations and quality units to resolve data inconsistencies obtain missing information and ensure that safety records remain aligned with current product and study documentation.Follow hybrid work model expectations by maintaining clear communication channels using digital collaboration tools effectively and safeguarding confidential safety data in both on site and remote work settings.Adhere to internal standard operating procedures and global pharmacovigilance guidelines by completing mandatory trainings documenting case handling steps thoroughly and supporting audit ready safety systems.Contribute to continuous improvement of case processing practices by sharing operational observations suggesting refinements to templates or workflows and supporting implementation of approved process enhancements.Support periodic review activities and safety summaries by providing reliable case level outputs that help medical safety experts evaluate trends and inform risk mitigation measures for patients and healthcare systems.Engage in knowledge building activities for pharmacovigilance and pharmaceutical research topics by participating in team discussions and learning sessions thereby strengthening personal expertise and overall team capability.
Qualifications
Demonstrate practical experience in pharmaceutical research and development activities with at least one year of exposure to clinical or safety related documentation that supports accurate medical data interpretation.Show familiarity with pharmacovigilance case processing concepts including data capture seriousness assessment and narrative preparation to enable effective handling of individual case safety reports.Apply foundational understanding of individual case safety report submission practices by following structured steps for dossier preparation and supporting timely reporting activities under supervision.Exhibit strong attention to detail in reviewing medical data adverse event descriptions and product information ensuring that safety records are complete consistent and suitable for regulatory use.Utilize effective written and verbal communication skills to collaborate with clinical safety and quality teams in a hybrid work environment while maintaining clear documentation of case related decisions.Demonstrate ability to work in a regulated environment by following pharmacovigilance procedures maintaining confidentiality of patient information and supporting compliance with global health authority expectations.Display motivation to expand knowledge in pharmacovigilance case processing and related safety sciences by engaging in training seeking feedback from experienced colleagues and applying learning to day to day tasks.
Certifications Required
Preferred certifications include pharmacovigilance or drug safety training from recognized industry bodies such as DIA or similar professional organizations.
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。
