Send Resumes to [email protected]

* *

Position: Statistical Programmer

Location: Fort Lee, NJ

Duration: Long term



*With at least 5 years experience in the pharmaceutical area. *

The primary responsibility of the statistical programmer is to support to
clinical trials for regulatory submission and publications; support
Biostatistics in statistical analysis, including generating analysis
datasets, patient listings, tables, and figures for clinical trials; develop
and maintain the infrastructure for project files of SAS datasets and SAS
codes.


Principle Responsibilities:
- Develop SAS programs including SAS macro programs to produce analysis
datasets, tables, listings and figures in support of statistical analysis
report based on CDISC compliant datasets
- Develop SAS programs for QC/validation to datasets, tables, listings and
figures produced
- Write/Review data definition tables, data specs or related documents
- Interacting with all functional groups and being a core member of an
inter-departmental team
- Design/develop SAS macros and other utilities to expedite SAS programming
activities
- Follow SOPs and good programming practices, adequately document programs
- Participate in statistical program validation and quality control
activities
- Quality Assurance on team member???s work and mentoring junior team
members when required

*Qualifications:*
- Minimum of 5 years programming in pharma industry
- Proficient in SAS/BASE, STAT, GRAPHICS, and MACRO
- Extensive experience with creating all files data, tables, figures, and
listings, documents, and analyses necessary to support an electronic
submissions and publications
- Familiarity with clinical trial design and analysis activities and basic
knowledge of regulatory guidelines FDA/CFR, ICH/GCP
- Experience in CNS preferred





Thanks & Regards

Adem
Technical Recruiter
Vertigon Consulting
Phone: 201-402-1610
Fax: 732-398-0506
Email: [email protected]

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