Job Summary
Join our dynamic team as a Pharmacovigilance Analyst in the Pharma Research & Development sector. In this role, you will play a critical part in ensuring the safety and efficacy of pharmaceutical products through the monitoring, evaluation, and analysis of drug safety data. Working closely with cross-functional teams, regulatory authorities, and internal stakeholders, you will support pharmacovigilance activities and contribute to maintaining compliance with global regulatory requirements.
Responsibilities
- Monitor and evaluate adverse event reports to ensure compliance with pharmacovigilance regulations and internal procedures.
- Collaborate with cross-functional teams to analyze, interpret, and communicate safety data effectively.
- Prepare safety reports and support regulatory submissions in accordance with applicable guidelines and timelines.
- Assist in the development, maintenance, and continuous improvement of pharmacovigilance systems and processes.
- Conduct literature reviews and surveillance activities to identify potential safety signals and emerging risks.
- Support PV case processing activities while ensuring data quality, accuracy, and completeness.
- Contribute to risk assessment and safety monitoring activities for pharmaceutical products.
- Maintain accurate documentation and records to support audits, inspections, and regulatory compliance.
- Participate in process improvement initiatives to enhance operational efficiency and effectiveness.
- Stay current with pharmacovigilance regulations, industry trends, and best practices.
Qualifications
- Degree in a relevant scientific discipline such as Life Sciences, Pharmacy, Medicine, Nursing, or a related field.
- Experience in Pharma Research & Development.
- Strong analytical and problem-solving skills with the ability to interpret complex safety data.
- Proficiency in pharmacovigilance data management and safety databases.
- Excellent communication and teamwork skills, with the ability to collaborate across multiple stakeholders.
- Experience in PV Case Processing.
- Certification in Pharmacovigilance or Drug Safety Management is preferred.
- Familiarity with risk management plans, safety assessments, and signal detection activities.
- Up-to-date knowledge of pharmacovigilance regulations, guidelines, and industry standards.
- Ability to mentor and support junior team members.
- Strong attention to detail and commitment to maintaining high-quality standards.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
Work Model
We believe hybrid work is the way forward as we strive to provide flexibility wherever possible. Based on this role's business requirements, this is a hybrid position requiring 2–3 days a week in a Cognizant office in Sao Paulo, BR. Regardless of your working arrangement, we are here to support a healthy work-life balance through our various wellbeing programs.
Benefits
- A career in one of the largest and fastest-growing IT services providers worldwide.
- Ongoing support and funding with training and development plans.
- Opportunity to work for leading global companies.
- A diverse, collaborative, and inclusive work environment.
- Highly competitive salary and benefits, including OSDE for you and your primary family group, annual bonus, and more.
Certifications Required
- Certification in Pharmacovigilance or Drug Safety Management (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。
