Job Description Sr Stat Pgmr - Welcome to MSUG: Michigan ...

Job Description

We have several permanent openings for Senior Statistical Programmers to work home-based

Candidates must have R programming experience; Oncology exp a plus.

(Some positions do not require R programming experience so please apply if you are otherwise qualified. If you have R programming background, please specify in your application)

Sr. Statistical Programmer

Purpose of Job:

The Senior Statistical Programmer is a member of the Biostatistics team and plays a lead role in performing all SAS programming tasks required for clinical trial analysis and reporting. This position works closely with other members of the Biostatistics, and Data Management departments on various clinical projects. May function as Lead Statistical Programmer on multiple projects.

Job Components/Major Responsibilities:

This job description serves only as a broad outline of the duties required and will be renewed and amended at periodic intervals in consultation with the Director, Statistical Programming.

? Manage or lead assignments and programming personnel on single or multiple projects.

? Mentor and train selected associates within the Statistical Programming group.

? Participates in the development of and ensures compliance to Standard Operating Procedures (SOPs), policies, and guidelines.

? Remain informed of new developments in programming that are relevant to the industry and contribute to the innovation of new reporting systems.

? Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.

? Develop standard macros and/or tools in SAS for data analysis and reporting.

? Assist with statistical quality assurance review.

? Review deliverables before transfer to either internal or external clients.

? Ensure that SAS programs developed for specific protocols are effectively portable to other protocols (Reusable code).

? Communicate to management on project status and resource issues.

? Direct the work of statistical programming services across sites to achieve quality, timely, and costeffective study deliverables.

? Solicit feedback on project profitability from manager or project manager in order to assess and address productivity issues.

? May contribute to performance reviews of statistical programmers.

Qualifications:

? MS degree required

? Experience leading SAS programming projects in the pharmaceutical industry demonstrated by the ability to independently act as the point of contact on the statistical programming for all phases of clinical trials, directing the work of one or more programmers.

? Proficient in industry standards, medical terminology, and clinical trial methodologies.

? Possess project management skills within the Statistical Programming function.

Company Description

At inVentiv Clinical Solutions (iCS), our mission is to be the alternative to traditional clinical outsourcing for the biopharmaceutical industry, allowing clients the greatest control and flexibility through unmatched access to the highest quality clinical resources. iCS provides clients with a variety of flexible options to meet their clinical trial objectives, including outsourcing of one or several functions associated with the clinical trial process, expert clinical staffing and recruitment, and creating strategically resourced work groups. Our solutions are designed to increase efficiency and accelerate results. iCS is headquartered in Houston, Texas, with offices throughout the globe.

Contact:

Anissa Rogers PharmaNet/i3 arogers@pharmanet-

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