PPD中国招聘火热进行中 - SAS Programmer & Biostatistician!-经管之家官网!

人大经济论坛-经管之家 收藏本站
您当前的位置> 软件培训>>

SAS软件培训

>>

PPD中国招聘火热进行中 - SAS Programmer & Biostatistician!

PPD中国招聘火热进行中 - SAS Programmer & Biostatistician!

发布:PPD-China | 分类:SAS软件培训

关于本站

人大经济论坛-经管之家:分享大学、考研、论文、会计、留学、数据、经济学、金融学、管理学、统计学、博弈论、统计年鉴、行业分析包括等相关资源。
经管之家是国内活跃的在线教育咨询平台!

经管之家新媒体交易平台

提供"微信号、微博、抖音、快手、头条、小红书、百家号、企鹅号、UC号、一点资讯"等虚拟账号交易,真正实现买卖双方的共赢。【请点击这里访问】

提供微信号、微博、抖音、快手、头条、小红书、百家号、企鹅号、UC号、一点资讯等虚拟账号交易,真正实现买卖双方的共赢。【请点击这里访问】

Pleaseconactusviaseven.shen@ppdi.comProgrammersAnalystKeywordsSAS,C++,JAVA,PROGRAMMING,STATISTICS,MATHEMATICSMajorRequired:ITpreferred.OthermajorslikeMathematics,Statistics,Engineering,Physicsareaccep ...
免费学术公开课,扫码加入


Please conact us via seven.shen@ppdi.com

Programmers Analyst

Key words
SAS, C++, JAVA, PROGRAMMING, STATISTICS, MATHEMATICS


Major Required:
IT preferred. Other majors like Mathematics, Statistics, Engineering, Physics are acceptable if have strong IT (ORACLE, JAVA, C++) and English background.

Essential Responsibilities
1. Develops SAS programs to produce data listings and Case Report Form Tabulations (CRT)
2. Builds standard tabulation datasets
3. Creates derived or analysis datasets
4. Develops SAS programs to implement statistical analyses to generate tables, listings and figures as specified in the statistical analysis plans
5. Performs validation of and quality assurance aspects of all SAS programming activities
6. Develops SAS programs for other needs
7. Consults on other statistical programming tasks, such as support for CRF design, database development, data validation plan and blinded data review.


Qualifications/Requirements:
1. Excellent English communication skills, can work independently with native English speaker.
2. Must have proficient SAS or Oracle SQL programming skills, if have neither of these two, must have a demonstrated capabilities to program in advanced languages: like C++, JAVA and/or assembly language.
3. Must possess great interpersonal capabilities and can work with people from different cultures. Have ability to construct good relationship within a team environment.
4. IT background preferred. Candidates from other majors with strong records and strong intention to be a programmer analyst are also welcomed.
5. Must have a bachelor degree, higher degrees are preferred.
6. Knowing drug development procedures and FDA/SFDA regulations is a plus.
7. Oversea working experiencein IT, Statistics, Math is a plus.
8. If apply for Sr. or Manager level position , must also have broad clinical trial background and have a knowledge of government regulations on drug development procedures, exempt for other levels.


Biostatistician

Responsibilities

Performs statistical activities for given clinical trials involving drugs, biologics and medical devices; provides statistical support to the project team; lead a biostatistics project tem.

Participates in clinical trial protocol development, including sample size and statistical power calculation and contribution to writing appropriate protocol sections.

Generates randomization schedule and participate drug repackage/relabeling activity.

Develops statistical analysis plan (SAP) including table shells design.

Reviews protocols, SAP or other study documents developed by other statistician(s) or consultant(s) and provides comments.

Represents statistical team at project team meetings and provides updates to project team on status of tasks.

Writes statistical analysis report (SAR) and participates in clinical study report (CSR) writing.

Performs other statistical review, such as case report form (CRF) design, database development, data validation plan and blinded data review report.

Where applicable, provides input and review the specifications of the programs that produce the tables, listings, figures, and/or analysis datasets.

Reviews and validates programs according to established departmental or partner’s procedures.

Performs other duties assigned by manager.

Qualifications

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

A minimum of 1 years experience of statistical and/or statistical programming applied to drug or medical device development

Knowledge, Skills and Abilities:

Good writing skills required to be able to write sections of protocols, statistical reports, clinical study reports, and randomization plans

Good SAS® programming skills.

Being familiar with CDISC data standards is a plus.

Experience of international drug development in a multicultural environment is a plus.

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

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

Good communication and interpersonal skills.

Be able to make effective presentations in public settings.

Proficient working in a PC/Windows environment.

Sufficient written and oral English communication skills.


「经管之家」APP:经管人学习、答疑、交友,就上经管之家!
免流量费下载资料----在经管之家app可以下载论坛上的所有资源,并且不额外收取下载高峰期的论坛币。
涵盖所有经管领域的优秀内容----覆盖经济、管理、金融投资、计量统计、数据分析、国贸、财会等专业的学习宝库,各类资料应有尽有。
来自五湖四海的经管达人----已经有上千万的经管人来到这里,你可以找到任何学科方向、有共同话题的朋友。
经管之家(原人大经济论坛),跨越高校的围墙,带你走进经管知识的新世界。
扫描下方二维码下载并注册APP
本文关键词:

本文论坛网址:https://bbs.pinggu.org/thread-1489108-1-1.html

人气文章

1.凡人大经济论坛-经管之家转载的文章,均出自其它媒体或其他官网介绍,目的在于传递更多的信息,并不代表本站赞同其观点和其真实性负责;
2.转载的文章仅代表原创作者观点,与本站无关。其原创性以及文中陈述文字和内容未经本站证实,本站对该文以及其中全部或者部分内容、文字的真实性、完整性、及时性,不作出任何保证或承若;
3.如本站转载稿涉及版权等问题,请作者及时联系本站,我们会及时处理。
经管之家 人大经济论坛 大学 专业 手机版