Statistical Programmer Analyst Job

SENIOR STATISTICAL PROGRAMMER ANALYST needed for a CONTRACT opportunity with Yoh's client located in San Francisco, CA.

TOP SKILLS SHOULD YOU POSSESS:

- Clinical Trial Knowledge
- Data Management
- Statistical Programming

WHAT YOU'LL BE DOING:

- Provide statistical programming expertise and hands on support to clinical projects across multiple therapeutics areas.
- Provide strong technical programming support to Biometrics and Data management.
- Contribute to activities in statistical systems development, validation and implementation including Standard Reporting Systems, SAS macro utility programs and associated tools.
- Perform vendor qualifications in regards to statistical programming function and oversees and validate vendor's programming activities such as CDISC implementation, analysis files specifications, and analysis, and programming conventions.
- Work closely with Data Management to assure data quality by providing ad-hoc analysis.
- Work closely with Biostatistics to create analysis files specifications and analysis outputs (TFL) following the instructions provided in Statistical Analysis Plan (SAP).
- Acts independently to determine methods and procedures on new assignments.
- Responsible for processing of clinical data required for analysis of clinical trials for Phase 1-4.
- Develop SAS coding and table templates for preparing, processing and analysing clinical data.
- Generate and QC summary tables, data listings and graphs for in-house analyses of study data or publications using SAS standard coding practices.
- Create/acquire tools to improve programming efficiency or quality.
- Validate work of other programmer/analysts at CRO or in-house.
- Create/review programming plan, specifications for datasets and TLFs.
- Familiar with CDISC conventions, ie, SDTM and ADaM models and hands on experience implementing these models.
- NDA submission experience is plus.
- Work with other functional groups to identify areas where statistical programming support can enhance efficiency and quality.
- Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
- Support data queries from other functional group (Medical Writing, Clinical Development, Clinical Operations, Regulatory, and Marketing).

WHAT YOU NEED TO BRING TO THE TABLE:

- A minimum of a Bachelor's degree in Computer Science, Mathematics, Statistics, and related areas is required.
- Equivalent experience may be accepted.
- A minimum eight (8) years hands on relevant career experience in the pharmaceutical or biotechnology industry.
- Excellent knowledge of SAS programming and associated features and their applications in pharmaceuticals industry environment in particular clinical trial data setting.
- Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
- Track record of generating new ideas and solutions to data analysis.
- Excellent application development skills.
- Thorough understanding of relational database components and theory.
- Excellent oral and written communication skills.

BONUS POINTS! OTHERWISE KNOWN AS PREFERRED QUALIFICATIONS:

- A Masters or PhD is preferred.

WHAT ARE YOU WAITING FOR? APPLY NOW!

RECRUITER: Will Thompson

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TAX TERM: CON_W2J2WPACNW

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