Job Summary
Serve as a specialist professional in pharmacovigilance within a hybrid work model supporting pharma research and development activities focused on the safe and effective use of medicinal products. Contribute to data driven safety evaluation and collaborate across functions to enhance patient safety outcomes and regulatory compliance.
Responsibilities
Perform end to end case related pharmacovigilance activities that support ongoing pharma research and development and help ensure timely safety reporting to regulatory bodiesReview available clinical and post marketing safety information to identify potential safety signals and contribute to risk assessment activities that protect patientsAnalyze safety data using company systems to detect trends or patterns and escalate relevant findings to medical safety experts for further evaluationDocument all safety case handling steps with clear and accurate narratives that enable transparent audits and inspections by internal and external stakeholdersCollaborate with cross functional research and development teams to integrate safety insights into study design and product lifecycle decisions that advance therapeutic innovationCoordinate with quality and compliance teams to follow current pharmacovigilance procedures and support continuous improvement of standard operating processesSupport preparation of safety sections for regulatory submissions and periodic reports so that product safety profiles are clearly communicated and well justifiedContribute to knowledge sharing sessions with peers to promote consistent case processing practices and strengthen the overall pharmacovigilance capability of the organizationEngage with internal technology and data teams to refine pharmacovigilance tools so that safety data capture and retrieval become more efficient and reliableParticipate in internal audits or readiness activities by providing case related documentation and clarifications that demonstrate strong adherence to pharmacovigilance requirementsAdapt work practices to a hybrid model by using digital collaboration platforms that maintain continuity of pharmacovigilance operations across onsite and remote settingsSupport broader company goals by transforming safety data into meaningful insights that guide responsible use of medicines and create a positive impact on public healthManage personal workload within day shift expectations to ensure all assigned safety activities and timelines are met without the need for travel
Qualifications
Possess a degree in life sciences pharmacy medicine or a related discipline that provides a solid scientific foundation for evaluating drug safety informationDemonstrate two to four years of focused experience in pharma research and development with direct exposure to pharmacovigilance practices and processesApply working knowledge of safety data review tools or databases to manage cases efficiently while maintaining data integrity and traceabilityUtilize familiarity with pharmacovigilance data management concepts to support accurate entry reconciliation and retrieval of safety information when requiredExhibit practical understanding of pharmacovigilance case processing steps including intake coding assessment and follow up activities that align with current regulationsCommunicate clearly in written and spoken form with global stakeholders to ensure that complex safety issues are documented and discussed in an accessible mannerShow commitment to ongoing learning about evolving pharmacovigilance guidelines and research methodologies so professional skills remain current and adaptable
Certifications Required
Desired certification in pharmacovigilance or drug safety such as a recognized pharmacovigilance professional credential
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。
