标题: PPD China Job Opportunity 诚招Sr./Biostatistician (Shanghai) [打印本页] 作者: shiyiming 时间: 2010-9-19 14:04 标题: PPD China Job Opportunity 诚招Sr./Biostatistician (Shanghai) PPD 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. More career information, please launch on <!-- m --><a class="postlink" href="http://www.ppdi.com">http://www.ppdi.com</a><!-- m -->.
Segment: Data Management & Biostatistician deparment, PPD China Shanghai
Position: Senior Biostatistician
Reporting to: Manager of Statistics
Responsibilities:
Performs statistical activities for given clinical trials involving drugs, biologics and medical devices, assist to oversee the activities of statistician consultants and provides technical support to the team.
Qualifications:
Ø An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field
Ø A minimum of 4 years (for M.S.) or 2 years (for Ph.D.) experience of statistical and/or statistical programming in CRO or pharmaceutical R&D including all phases and large studies applied to drug or medical device development
Knowledge, Skills and Abilities:
Ø Strong writing skills required to be able to write sections of protocols, statistical reports, clinical study reports, and randomization plans
Ø SAS® programming skills and familiarity of other statistical packages (e.g. StatXact, nQuery) and understanding of database structures
Ø Experience of international drug development in a multicultural environment is a plus
Ø Being familiar with CDISC data standards is a plus
Ø Excellence in planning, managing and coordinating statistical and statistical programming activities in clinical trials; previous management experience of statisticians is preferred
Ø Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
Ø Excellent communication and interpersonal skills
Ø Sufficient active written and oral English communication skills
Performs statistical activities for given clinical trials involving drugs, biologics and medical devices; provides statistical support to the project team. (see the attached JD for the details of responsibility)
Qualifications:
Ø An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field
Ø A minimum of 1 years experience of statistical and/or statistical programming applied to drug or medical device development
Knowledge, Skills and Abilities:
Ø Good writing skills required to be able to write sections of protocols, statistical reports, clinical study reports, and randomization plans
Ø SAS® programming skills, familiarity of other statistical packages e.g. StatXact, nQuery) and understanding of database structures.
Ø Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
Ø Good communication and interpersonal skills
Ø Sufficient written and oral English communication skills
Interested? Send your application resume to <!-- e --><a href="mailto:li.yan@ppdi.com">li.yan@ppdi.com</a><!-- e --> for your career now!