Job Summary
This hybrid day shift role for TL Pharmacovigilance focuses on end-to-end safety oversight across pharma research and development activities, coordinating PV data management and case processing to ensure accurate reporting, regulatory compliance, and continuous risk evaluation. The role demands 4 to 6 years of experience and enables impactful contributions to patient safety and innovation.
Responsibilities
- Responsible for day-to-day work.
- Tracking of activities daily for the project.
- Timely reporting of metrics and updating related quality tools/trackers for deliverables. Setting performance goals for the team.
- Maintenance of case tracking sheets for billing and deliverables.
- Ensure appropriate distribution of work among direct reports.
- Ensure proper communication with client (as applicable).
- Ensure completion of training plan and mentoring documentation archival for all direct reports.
- Mentoring and coaching of the team as well as the new hires on a regular basis or as required.
- Ensure that SLAs and KPIs are maintained as per contractual agreement.
- Perform annual performance appraisals of direct reports and provide regular feedback to the team.
- Reporting to their supervisor on performance, status, and any escalations for the team.
- Responsible for motivation and retention of the team.
- Communication of resource issues/resignations/absconder to supervisor.
- Managing assessment and development of team members.
- Ensure audit readiness at all times.
- Ensure adherence to internal and client procedures for self and team.
- Ensuring training compliance and proper documentation is maintained.
- Lead/guide associates in process improvement initiatives in agreement with client.
Basic Qualifications
- Graduate/Postgraduate/Doctorate degree in Life Sciences, Science, Healthcare, Pharmacy, Medical Sciences, or equivalent degree.
- Minimum 3 years of total experience in PV and/or the pharmaceutical/clinical field, including:
- Minimum 1 year of experience handling teams for external hires, or
- Minimum 2 years of experience in the Novartis engagement for internal promotion/re-hire.
- Fluency in English.
- Effective communication skills.
- Ability to perform tasks accurately and in a timely manner.
- Leadership and people management skills.
- Self and team motivation.
- Result-oriented.
- Metric management.
Certifications Required
- Preferred certification in pharmacovigilance or drug safety, such as DSRM or equivalent industry-recognized PV 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。







