Lead SAS Programmer - Genzyme Corporation (Cambridge, MA)

Salary: 90-120/hour Industry: Clinical Trials Job Description

Currently, we are looking to staff (2) SAS Programming roles that require at least 7 years of experience which includes prior submissions experience.

• There is a $2,000.00 referral bonus for every referral that we can place here at Genzyme.
• We pay the bonus after the referral candidate is hired and has successfully completed 90 days with Randstad/Genzyme.

Job Description:

Submissions SAS Programmer-

• Provide submission preparation and QC support for dataset section of submissions. QC datasets, documentation, programs, etc. to ensure submission readiness. Track all variables to source/origin and ensure documented clearly either on annotated CRF, external data documentation, or analysis dataset documentation. Ensure algorithms of derived variables adequately described in dataset documentation. Provide publishing support for preparation of define PDF files. Provide QC of draft published dataset content to ensure submission readiness. Provides support to Manager of Clinical Data Services and work with project team statisticians and SAS Programmers on the submission preparation of content for dataset section of submissions across many products. This is a contract role through Randstad and we will only consider consultants who are willing to work on a W-2 basis through Randstad. The hourly pay rate range is largely based on experience but the rate range is 90-120/hour. We do not relocated any candidates and do not sponsor visas.
• Requires high (principal or senior) level SAS programming skills and good understanding of regulatory requirements for datasets for submission.
• Certification in SAS is highly desired. Needs to be detail and quality oriented. Good communication skills necessary. Familiarity with publishing tools such as Adobe Acrobat a plus. Works under the oversight of the Manager of Clinical Data Services.

If you know of anyone looking for a new challenge that fits the job description above, please let me know and as always, I appreciate your referrals. I wish you continued success in 2008.

Qualifications

Requires high (principal or senior) level SAS programming skills and good understanding of regulatory requirements for datasets for submission.

Certification in SAS is highly desired. Needs to be detail and quality oriented. Good communication skills necessary. Familiarity with publishing tools such as Adobe Acrobat a plus. Works under the oversight of the Manager of Clinical Data Services.

Organization

Reports into the BioMedical Operations organization and specifically, the Statistical Programming team. www.genzyme.com Contact: kathleen.mcteague [at] genzyme.com Company: Randstad at Genzyme

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