Biostatistician 生物统计师招聘_精鼎医药研究开发（上海）有限公司最新招聘信息-猎才医药网

职位描述

职位描述： *Job DescriptionAt PAREXEL, we believe that the power to work independently and intelligently should be yours every day.Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. PAREXEL Biostatistics units have an excellent reputation in the industry for their standards of work and quality of resultsAs a Biostatistician dedicated to late-phase clinical studies (e.g., Phase II - IV, “pragmatic” trials, observational studies, registries; outcomes research, ) you will lead research design and analytical strategies, input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts and provide statistical advice. You will input into the quality control of statistical deliverables. As the functional lead within a study team, you will lead the biostatistical and statistical programming activities on a study and be accountable for the deliverables from these functions. Key responsibilities also include project management of deliverables, resource and function specific budget. You will have the opportunity to become a subject matter expert for specific tasks within a key client partnership and to become involved in business development activities.An exciting and rewarding opportunity has arisen to join our international team asSenior/Principal BiostatisticianLocation - Berlin Germanyto contribute to contribute to meaningful advances that benefit patients in need.1 sentence quote from Hiring Manager about the job: You’ll be able to develop your statistical skills, working as a functional lead in dynamic teams. You’ll gain exposure to multiple therapeutic areas, have the opportunity to grow and develop your career and be part of a pleasant and flexible working environment.KEY RESPONSIBILITIES:? Perform or supervise complex statistical analyses and create or provide input to statistical reports – usually in English.? Cooperate with other biostatistical and company departments to optimize the global efficiency.? Act as a pro-active advisor for all types of analysis during the proposal process as well as during the project life cycle; define strategies and evaluate the statistical resources needed to meet the defined goals.? Coordinate Biostatistics related project activities for successful completion within given timelines and budget.? Interact with clients with regard to data analysis, scope of work, and budget.? Review derived datasets and all types of statistical analysis deliverables.? Develop complex analysis strategies, and execute them using efficient programming techniques (software: SAS).? Produce and provide expert input to analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.? Quality control of all kinds of statistical deliverables.? Training/mentoring of junior members of the department.? Representing PAREXEL at client meetings*Job QualificationsKEY QUALIFICATIONS:? Degree in Biostatistics/Statistics or relevant quantitative sciences degree and a Masters or PhD in a statistical subject.? You have a thorough understanding of statistical issues in both clinical trials (and other randomized experiments) and observational studies (e.g. comparative cohort studies, case-control, retrospective/prospective cohort).? You will have experience in statistical analysis in a clinically related subject, either within clinical trials or in Epidemiology, either academically or professionally – and/or Outcomes research.? Experience with oncology and/or diabetes trials would be an advantage.? You are able to work independently and in a team.? You are confident, self-reliant, and a quick learner.? You have advanced SAS programming skills.? Good oral and written English communication skills are mandatory.? Ability to travel as required?Starting your journey with PAREXEL comes along with an extensive induction program and ongoing training while following your individual career path. We have been recognized as a 2015 Training Top 125 by Training Magazine for our excellence in employer-sponsored training and development programs.On your PAREXEL journey, you will be involved in all statistical aspects of clinical trials, you will work in cross-functional teams, and with managers who know your strengths. If you’re looking for flexibility and work-life balance, we’re here to listen and help you move forward with your individual career path.There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. If you’re looking to collaborate with life science industry leaders, gain exposure to industry changing technology, and find the security of a role within a global CRO join a team that will help you move forward with your individual career path. 职能类别：其他关键字：统计 SAS

公司信息

精鼎医药研究开发(上海)有限公司(PAREXEL International)，成立于1982年，是一家致力于药物临床试验研究的CRO (Contract Research Organization)集团公司。总部位于美国，分支机构遍布欧、美、亚、大洋四大洲，且于亚洲13个国家和地区设立了分支机构，致力深耕于当地。精鼎医药由一群具有丰富跨国性临床试验研发经验及专业知识的精英所组成，服务团队集合各种不同专业领域的人才。我们重视与客户的承诺，更重视人才的培育和养成，我们提供完整的教育训练、职涯规划、优于市场的薪资福利、良好工作环境，期许同仁与公司一同成长，迈向未来。愿景（Vision）：创造一个在亚太地区具有国际竞争力的最精良CRO团队。发展使命（Mission）： 1．争取国际大药厂委托，执行符合国际水准的跨国性临床试验。 2．协助亚太生技及制药产业建立新药开发模式，以提升产品研发能力，幷促使产品国际化。 3．以提升临床试验品质为宗旨，拓展全球市场为目标，整合计算机及通讯科技，在国际上提供客户兼具成本效益及效率的临床试验数据处理中心。 4．建立一个以亚洲人种高发生率疾病的基因数据库，以提供国际性新药研发机构所须之基因信息，协助其缩短药物开发时程，幷提高研发成功率。公司福利和人才培养计划：保险类： 1. 社会保险(依照国家规定)及住房公积金； 2. 团体保险（包括寿险、意外暨医疗保险）； 3. 补充医疗保险；制度类： 1. 学习发展计划 (Learning & Development): 针对个别员工之专业及兴趣，设计符合其个人之生涯规划； 2. 完整的教育训练：每年公司均针对所有员工，提供完整之教育训练； 3. 顺畅的升迁管道及可转调其它部门；如有职缺，亦可申请调至海外各子公司；请 / 休假制度： 1. 服务第一年即享有14天年假, 后续年休假天数则依据服务年资及公司制度而定； 2. 一年可享12天不扣薪病假； 3. 员工旅游, 年度体检；精鼎医药将以培养国际性的人才为目标，欢迎具有国际观之人才加入。应聘方法： 1. 在线投递； 2. 请登录我们的公司网站直接投您的简历（https://jobs.parexel.com/search-jobs）我们在收到您的简历之后，会尽快与您联系。谢谢！

周边城市招聘：上海浙江安徽广东山东河北重庆北京江苏湖南

企业入驻日期： 2017-11-09

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