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Company
PPD (Pharmaceutical Product Development, Inc.)
Business Segment
PPD-Biometrics, Shanghai Office
Job Title
Programmer Analyst or Sr. Programmer Analyst
Location
Shanghai, China P.R.
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 experience in 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.
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Job Title
Biostatistician or Sr. Biostatistician
Location
Shanghai, China P.R.
Key words
SAS, PROGRAMMING, STATISTICS, MATHEMATICS
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:
An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field
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:
Strong writing skills required to be able to write sections of protocols, statistical reports, clinical study reports, and randomization plans
SAS programming skills and familiarity of other statistical packages (e.g. StatXact, nQuery) and understanding of database structures
Experience of international drug development in a multicultural environment is a plus
Being familiar with CDISC data standards is a plus
Excellence in planning, managing and coordinating statistical and statistical programming activities in clinical trials; previous management experience of statisticians is preferred
Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
Excellent communication and interpersonal skills
Sufficient active written and oral English communication skills
Position: Biostatistician
Reporting to: Manager of Statistics
Responsibilities
Performs statistical activities for given clinical trials involving drugs, biologics and medical devices; provides statistical support to the project team.
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
SAS? programming skills, familiarity of other statistical packages e.g. StatXact, nQuery) and understanding of database structures.
Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
Good communication and interpersonal skills
Sufficient written and oral English communication skills
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