Job Summary
Data - Join our dynamic team as a Pharmacovigilance Specialist where you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With a focus on Pharma Research and Development you will contribute to the monitoring and reporting of drug safety data. This hybrid role offers a rotational shift schedule providing flexibility and the opportunity to make a significant impact on public health.
Responsibilities
- Monitor and evaluate adverse event reports to ensure compliance with regulatory requirements and company standards.
- Collaborate with cross-functional teams to analyze safety data and identify potential safety signals.
- Prepare and submit aggregate reports such as PSURs to regulatory authorities in a timely manner.
- Conduct thorough research and development activities to support the safety profile of pharmaceutical products.
- Utilize your expertise in Pharmacovigilance and Safety Operations to enhance drug safety monitoring processes.
- Provide technical guidance and support to team members in the analysis and interpretation of safety data.
- Develop and implement strategies to improve the efficiency and effectiveness of safety reporting systems.
- Ensure accurate documentation and maintenance of safety data in compliance with regulatory guidelines.
- Participate in the development and review of standard operating procedures related to pharmacovigilance activities.
- Collaborate with stakeholders to address safety-related inquiries and provide expert advice.
- Contribute to the continuous improvement of pharmacovigilance processes and systems.
- Support the training and development of team members in pharmacovigilance practices.
- Engage in regular communication with regulatory authorities to ensure alignment on safety reporting requirements.
Qualifications
- Possess a strong background in Pharma Research and Development with a minimum of 4 years of experience.
- Demonstrate expertise in Aggregate (PSUR) reporting and Pharmacovigilance and Safety Operations.
- Exhibit proficiency in analyzing and interpreting complex safety data.
- Display excellent communication and collaboration skills to work effectively in a hybrid work model.
- Show adaptability to rotational shifts and a commitment to maintaining high standards of safety reporting.
- Hold a relevant certification in Pharmacovigilance or a related field.
Certifications Required
Certified Pharmacovigilance Professional (CPP) or equivalent 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。
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