Office Location: Budapest, Hungary – 9th District, Mill Park Office Building
Working Hours: 40 hours per week
Work Arrangement: 100% Remote
Schedule: Standard business hours
What We Offer
- Competitive salary and cafeteria benefits
- Discounted All You Can Move SportPass
- Comprehensive medical benefits
- Risk and accident insurance coverage
- Opportunity to be part of a rapidly expanding organization
- Continuous training, learning, and certification opportunities
- Multilingual environment with native-speaking colleagues
- Inspiring and pleasant working atmosphere in a multicultural community
- Reimbursable language courses
Essential Qualifications
· Life-Science / Healthcare Professional / Master of Public Health with experience in Literature reviews / Pharmacoepidemiology / Master’s degree in Epidemiology
Preferred Working Experience:
· 2+ years’ experience in performing literature reviews in Epidemiology or Public Health
· Experience in statistical analysis software such as STATA or SAS etc.
Essential skills
· Demonstrates depth and breadth of specialist knowledge of epidemiology and medical statistics
· Demonstrates awareness of the critical appraisal of epidemiological literature and of different study designs commonly used in epidemiological studies
· Fluent English (oral and written)
· Good Understanding of epidemiology
· Experience performing critical commentaries of studies (limitations, implications and conclusions)
· Ability to critically appraise and synthesize epidemiological literature
· Ability to write research reports and to effectively disseminate outcome
· Strong interpersonal and communication skills
· Initiative for process improvement
· Ensure customer satisfaction
· Good team worker
· Good business ethics
· Literature reviews as requested by client epidemiologists using the best practice methodologies
· Literature search and preparation of Literature review report for Pharmacoepidemiology
Responsibilities
· Literature reviews as requested by client epidemiologists using the best practice methodologies
· Literature search and preparation of Literature review report for Pharmacoepidemiology
· Perform peer Scientific & Technical Review
· Follows the processes and requirements as outlined in the client guidance documents on Literature Reviews
· Provides review reports in format and quality as described in the guidance document
· To collaborate with the client epidemiologist(s) to define timelines for the literature reviews, to clarify questions, to provide feedback
· Understanding the disease area and therapeutics compound’s mode of action as applicable
· Attending, along with supervisor if required, Safety Management Team (SMT) meetings as applicable
· Discussing any comments regarding the literature review (including epidemiological interpretation) with the Safety Management Team SMT as applicable
· Working independently / directly / in consultation with Medical Writer, Regulatory Team, Global Pharmacovigilance Safety Lead or Scientific and Operational Epidemiology Lead for epidemiological evidence review projects i.e. drug Safety Profile Plans (dSPP), Risk Management Plans (RMP), Orphan Drug Application (ODA), Pregnancy and Lactation Labeling Rule (PLLR) updates or Pediatric Investigation Plans (PIP)
CogHU103
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。
