Collabera
SAS Programmer
Collabera, Jersey City, New Jersey, United States, 07390
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.Job Description
The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities.Perform role of primary and validation statistical programmer on all assigned studies, integrated summaries, and in support of responses to questions from regulatory authorities.Create derived data set specifications for all assigned studies and integrated summaries.Create data definition tables for analysis data sets for all assigned studies and integrated summaries.Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician.Review annotated case report forms and provide comments to study designer.Represent Statistical Programming on all assigned project and study teams as needed.Qualifications
3-5 years experience performing statistical programming with SAS in a pharmaceutical or CRO environment.Bachelor’s Degree or above in Statistics, Biostatistics, Mathematics, Computer Science, or another related field.Additional Information
To know more about this opportunity, please contact.
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The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities.Perform role of primary and validation statistical programmer on all assigned studies, integrated summaries, and in support of responses to questions from regulatory authorities.Create derived data set specifications for all assigned studies and integrated summaries.Create data definition tables for analysis data sets for all assigned studies and integrated summaries.Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician.Review annotated case report forms and provide comments to study designer.Represent Statistical Programming on all assigned project and study teams as needed.Qualifications
3-5 years experience performing statistical programming with SAS in a pharmaceutical or CRO environment.Bachelor’s Degree or above in Statistics, Biostatistics, Mathematics, Computer Science, or another related field.Additional Information
To know more about this opportunity, please contact.
#J-18808-Ljbffr