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A leading IT staffing firm seeks a Senior Statistical Programmer to lead statistical programming activities for clinical studies. The candidate will perform data set specifications and support regulatory submissions. Ideal applicants should have 3-5 years of experience with SAS and a relevant Bachelor's Degree.
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions), Permanent Placement Services, and Vendor Management Programs.
Collabera recognizes the true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental, and Vision insurance, 401K retirement savings plan, Life Insurance, and Disability Insurance.
If you are interested, give me a call at 973-606-3290 or send your resume to himanshu.prajapat(at)collabera.com
Position summary:
The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This includes statistical programming for clinical studies, integrated summaries, and supporting responses to regulatory authorities.
• Serve as primary and validation statistical programmer on all assigned studies, integrated summaries, and in support of regulatory questions.
• Create derived data set specifications for all assigned studies and summaries.
• Develop data definition tables for analysis data sets.
• Review statistical analysis plans and provide comments to biostatisticians.
• Review annotated case report forms and provide feedback to study designers.
• Represent Statistical Programming on project and study teams as needed.
• 3-5 years of experience in statistical programming with SAS in a pharmaceutical or CRO environment.
• Bachelor’s Degree or higher in Statistics, Biostatistics, Mathematics, Computer Science, or related fields.
To learn more about this opportunity, please contact us.