Paramax international 诚聘高级SAS程序员和统计师！

shiyiming

Paramax International Corporation is an international contract research organization providing full services to pharmaceuticals & institutes, since the inception in the United States in Jan.,2003, we have cooperated with many transnational pharmaceuticals in various therapeutical areas. This year we have established our offices in Beijing & Shanghai, China. Our business scope includes study planning, clinical study management, medical writing, regulatory affairs, clinical data management and biometrics.

As a fast-growing company, we provides the flexible, stimulating, and enjoyable work environment, competitive pay, good benefit, opportunities to advance, and job security. We view every staff as part of one big team and strive to work together. Currently we are looking for the new members to join our team.

If you are interested, please send your CV to <!-- e --><a href="mailto:hr@pmxintl.com">mailto:hr@pmxintl.com</a><!-- e -->. We will reply you within 15 working days upon receipt of your CV!

[u:f60a4]Senior SAS Programmer 高级SAS 程序员[/u:f60a4]

Key Responsibilities:
- Design, develop, and modify computer programs to store, analyze and evaluate clinical data;
- Perform peer review and validation of programming code;
- Support Data Management by planning, designing, validating, and documenting clinical databases;
- Support Biostatistics by providing datasets, tables, listings, and figures for Clinical Study Reports.

Qualifications:
- Bachelor degree or above in statistics, mathematics, computer science, or a related field;
- Over 3 years of SAS programming experience (including SAS Base/Macro/SQL/STAT/Graph) and/or Clintrial/Oracle/SQL programming experience;
- Experience producing deliverables for regulatory submissions using SAS (analysis datasets, tables, listings, graphs) and/or clinical trial databases using Clintrial/Oracle/SQL;
- Excellent spoken and written communication skills;
- Strong sense of responsibility and dedication;
- Teamwork spirit.

[u:f60a4]Biostatistician 统计专员[/u:f60a4]

Key Responsibilities:
- Provide input into clinical development activities from concept to study design and implementation;
- Generate or review randomization schedule;
- Perform and/or coordinate the preparation, execution, reporting and documentation of interim and final statistical analyses;
- Write or review SAPs & statistical report;
- Maintain expertise in state-of-the-art data manipulation and statistical analyses;
- Provide support for publication of clinical trial results.

Qualifications:
- Bachelor degree or above in biostatisitics or epidemiology;
- Over 2 years biostatistician experience;
- Good verbal and written communication skills;
- Proven ability to communicate in English;
- Strong sense of responsibility and dedication;
- Excellent interpersonal skills;
- Teamwork spirit.