Career

Associate Statistical Programmer 

Job Category: Biotechnology/Pharmaceutical

ID: P00001

Job Location: Guangzhou, China

Job Description

Responsible for SAS programming and QC activities for assigned projects of clinical trial studies under the supervision of biostatistician and Senior SAS Programmer

Prioritize personal workload to meet specified completion dates and perform work with supervision and direction

Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment

Education/Qualification

Bachelor degree or above in the major of Statistics, Biostatistics, Computing or Mathematical, etc

Basic knowledge of SAS, SQL and SAS macro

Good in written and verbal English, pass the CET-4 preferred

Experience

Basic knowledge of statistics

Effective communication skills

Proven ability to work in a team environment

Proven ability to work independently under supervision

Proven interpersonal skills

 

 

 

 

 

 

 

Statistical Programmer 

Job Category: Biotechnology/Pharmaceutical

ID: P00002

Job Location: Guangzhou, China

Job Description

Create Study Data Tabulation Model (SDTM)

Create Analysis Data Model (ADaM)

Develop SAS programs to produce data listings, tables and figures

Perform validation of all SAS programming activities

Assist in the production and QC of analysis plans, TFL developments, derived dataset specifications, programming specifications and the process supporting documents

Prioritize personal workload to meet specified completion dates and perform work with limited supervision and direction

Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment

Education/Qualification

Bachelor degree or above in the major of Statistics, Biostatistics, Computing or Mathematical, etc

Solid knowledge of SAS, SQL and SAS macro

Good in written and verbal English, can work with native English speaker, pass the CET-6 preferred

Experience

Basic knowledge of statistics and clinical trial process

A proactive approach to developing and maintaining effective working relationships with staff in other locations and in working to achieve consistent processes and standards across them

Good oral and written communication skills

Demonstrated ability to work in a team environment

Demonstrated ability to work independently under supervision

 

Senior Statistical Programmer 

Job Category: Biotechnology/Pharmaceutical

ID: P00003

Job Location: Guangzhou, China

Job Description

Good experience with CDISC standards

Develop SAS programs for SDTM, ADaM, client-defined analysis datasets, Tables, Listings and Figures, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) as specified in the SAP (Statistical Analysis Plan)

Perform validation and quality control of SAS programming activities

Provide technical planning to include overseeing the set-up of key macros and SAS programs.

Represent Statistical Programming at internal and client meetings

Act as a Statistical Programming Consultant to clients and internal customers in related disciplines e.g. Clinical Data Management, Project Management and Medical Writing

Prioritize personal and teammates workload 

Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment

Education/Qualification

Bachelor degree or above in the major of Statistics, Biostatistics, Computing or Mathematical, etc

Zero to three years experiences with demonstrated SAS skills within a clinical trials environment

Fluent in written and verbal English, can work independently with native English speaker, pass the CET-6 preferred

Experience

Knowledge of statistics, clinical trial process and data management, biometrics and systems applications to support operations preferred

Team leadership experience, as demonstrated by ability to organize and motivate project teams

Good time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of work

 

EEO Employer

LLX Solutions, LLC is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.

 

If you have the intention to apply, please send us your resume in both Chinese and English, and indicate the job title.

 

Waltham (Headquarters)

Address: 230 2nd Ave, Suite 140, Waltham, MA 

Zip Code: 02451

E-mail: clarissa.lion@llxsolutions.com