PPD公司(www.ppdi.com)是一家全球领先的合同制研究组织。提供发现，开发和批准后服务，以及复合伙伴关系计划。我们的客户和合作伙伴包括制药，生物技术，医疗设备，学术机构和政府组织。在33个国家拥有办事处，全球拥有超过10500专业人才，PPD运用创新技术、治疗领域的专业知识和对质量的承诺帮助其客户和合作伙伴实现最大化的R ＆ D投资收益，并为病人加快提供安全，有效的治疗方法。

    也许以您的技能和经验，您可能为您的职业生涯的道路提供多种选择。那么，为什么选择PPD？

  临床研究机构是非常令人振奋的行业，但同时做好也很有难度，竞争激烈。我

们知道，为了吸引最优秀和最聪明的员工，我们必须提供一个刺激和富有挑战性的环境。 PPD公司把雇员看作为其成功的关键所在，我们力争使PPD凝聚活力和充实的经验，使个人能够有所作为。

   如果你可能因选择PPD作为正确的职业而丧失你的年终奖金分红，我们将为您提供相当的签约奖金，激励您与我们开始！

   目前，在我们的北京,上海办事处有许多令人兴奋的机会。

PPD (www.ppdi.com) is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 33 countries and more than 10,500 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients.

With your skills and experience, you probably have several options for your professional career path. So, why choose PPD?

The CRO industry is exciting, but demanding and competitive. We know that to attract the best and the brightest we have to provide a stimulating and challenging environment. PPD recognizes its employees as the key to its success, and we strive to make PPD an energizing and fulfilling experience, where individuals can make a difference.

If you are in jeopardy of losing your year-end bonus payout for choosing the right career with PPD, we will provide you with a comparable sign-on bonus incentive for starting with us!

We currently have many exciting opportunities in our Beijing, Shanghai offices.

For all positions, a good command of spoken and written English is necessary.

To submit your application, please send your CV in English, with salary requirements and an indication of the position in which you are interested, to:li.yan@ppdi.com.

 JOB DESCRIPTION FOR Intern/Associate Programmer Analyst

Intern/Associate Programmer Analyst* (China)

Description

Duties and Responsibilities (according to relevant guidelines, laws and SOPs)

·            Become familiar with and follow the departmental and company standard operating procedures (SOPs) and working practices (WPs).

·            Ensure projects are well documented consistent with company SOPs and working practices.

·            Time management of own time spent on projects.

·            Contribute to statistical analysis plans, mainly through table, listing and graph specifications.

·            Provide programming support for the development and validation of the analysis database.

·            Provide support for the production of statistical appendices, with appropriate documentation.

·            Provide support for the validation of statistical appendices, with appropriate documentation.

Qualifications

Qualifications:                                   

BSc degree in statistics, computing or related field is desirable.

Skills and knowledge:                      

Computer literacy in one or more computer systems/packages (preferably SAS^®) and understanding of database structures.

Good organizational skills of own work load with the ability to adapt and adjust to changing priorities.

Excellent written and verbal communication skills.

Ability to contribute in a multi-disciplinary team setting.

Positive attitude and the ability to work well with others.

Experience:                                         

None, although some experience in a clinical research environment is preferred, as is experience in SAS^®.

Job

 Biostatistics

Primary Location

Asia Pacific-China-Beijing-Beijing

Other Locations

Asia Pacific-China-Shanghai-Shanghai

Job Description for INTERN/junior BioSTATISTICIAN

Performs biostatistical and programming activities for given clinical trials involving drugs, biologics and medical devices; assists higher level biostatisticians for project tasks.

Responsibilities

Ø  Assists in study design and development of statistical section in clinical trial protocols

Ø  Assists sample size and statistical power calculations and randomization schedule generation

Ø  Attributes to development of statistical analysis plans including table shells design for individual studies

Ø  Supports data safety monitoring board (DSMB) or data monitoring committee (DMC) and clinical endpoints committee (CEC) regarding to statistics analysis

Ø  Participate in statistical support for CRF design, database development, data validation plan and blinded data review

Ø  Performs SAS programming to generate tables, listings, figures, and statistical analyses

Ø  Assists higher level biostatisticians for the project tasks

Ø  Conducts literature searches to support statistical team

Ø  Performs other duties assigned by supervisor

Qualifications

Ø  An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field

Ø  Experience of statistical analysis in the pharmaceutical industry is preferred

Ø  Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality

Ø  Be knowledgeable in drug agencies (e.g. FDA) regulations and requirements governing the conduct of drug and medical device studies including, but not limited to, GCP and ICH requirements

Ø  Good communication and interpersonal skills

Ø  Proficient working in a PC/Windows environment

Ø  A good command of English language if one’s native language is not English

感兴趣公司的职位，请直接发送个人简历到：li.yan@ppdi.com（不接受附件申请）,

邮件名称：姓名 – 职位 – 城市。