Katalyst CRO
Overview
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Senior SAS Programmer
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Katalyst CRO Responsibilities
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. Perform data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/Client), utilizing SAS programming. Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs). Production and QC / validation programming. Generate complex ad-hoc reports utilizing raw data. Apply a strong understanding/experience of Efficacy analysis. Create and review submission documents and eCRTs. Communicate with and/or respond to internal cross-functional teams and clients for project specifications, status, issues or inquiries. Perform lead duties when called upon. Serve as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc. Be adaptable and flexible when priorities change. Requirements
Bachelor's degree in Statistics, Computer Science, Mathematics, or a related field. 7 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree, or 6 years with a master’s degree. Strong SAS data manipulation, analysis and reporting skills. Good working knowledge of R and have applied it in clinical trial analysis. Solid experience implementing the latest CDISC SDTM / ADaM standards. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis. Familiarity with the drug development life cycle and experience with manipulation, analysis and reporting of clinical trials data. Submissions experience utilizing define.xml and other submission documents. Excellent analytical & troubleshooting skills. Ability to provide quality output and deliverables, in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. Seniority level
Mid-Senior level Employment type
Contract Job function
Information Technology Industries
Pharmaceutical Manufacturing
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Join to apply for the
Senior SAS Programmer
role at
Katalyst CRO Responsibilities
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. Perform data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/Client), utilizing SAS programming. Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs). Production and QC / validation programming. Generate complex ad-hoc reports utilizing raw data. Apply a strong understanding/experience of Efficacy analysis. Create and review submission documents and eCRTs. Communicate with and/or respond to internal cross-functional teams and clients for project specifications, status, issues or inquiries. Perform lead duties when called upon. Serve as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc. Be adaptable and flexible when priorities change. Requirements
Bachelor's degree in Statistics, Computer Science, Mathematics, or a related field. 7 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree, or 6 years with a master’s degree. Strong SAS data manipulation, analysis and reporting skills. Good working knowledge of R and have applied it in clinical trial analysis. Solid experience implementing the latest CDISC SDTM / ADaM standards. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis. Familiarity with the drug development life cycle and experience with manipulation, analysis and reporting of clinical trials data. Submissions experience utilizing define.xml and other submission documents. Excellent analytical & troubleshooting skills. Ability to provide quality output and deliverables, in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. Seniority level
Mid-Senior level Employment type
Contract Job function
Information Technology Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr