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
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。
