US Tech Solutions, Inc.
Principal Statistical Programmer
US Tech Solutions, Inc., Atlanta, Georgia, United States, 30383
Duration: 6 months contract
Remote
Job Description
Under the supervision of the Head of Statistical Programming, the Contractor Statistical Programmer will be assigned to work on a TA / Study at Client. The contractor will participate in the oversight, creation, maintenance and finalization of clinical study datasets / TFL for Client development programs, and ensure all clinical datasets perform the analysis defined by SAP and meet the standards required for regulatory submissions for all INDs and NDAs / MAAs
Responsibilities
Responsible for Statistical Programming activities, including analyzing, integrating and reporting of clinical trial data in order to produce quality and timely deliverables.
Performs data analysis using primarily the SAS programming language for the summary and interpretation of clinical trial data.
Provide statistical programming support to generate derived analysis data sets, tables, listings, and figures for Clinical Study Reports, regulatory submissions, annual IND safety update reports and Integrated summaries (ISS / ISE).
Creation / QC of CDISC SDTM and ADaM files, SAS export files and Define.xml use for Electronic Submission from the data received in non-standard form from various sources.
Interact with Statisticians, Programmers and other members of the clinical team, perform ad hoc analysis and generate outputs according to the requirements.
Review and comment on CRFs, annotated CRFs, Data Management Plan, Data validation plan, edit check specifications and study related documents.
Participate in operations meetings and address issues that may influence statistical programming and data management.
Work with CRO statisticians, statistical programmers and review / QC their work / deliveries.
Experience
5+ years’ programming experience in pharmaceutical / biotech / CRO environment in drug discovery / clinical trials / drug development
Experience in working with multidisciplinary groups (internal & external), flexibility, adaptability and ability skills to work within a matrix environment.
Skills
Proficiency in statistical programming package(s), SAS is required ; R or other packages are desired.
Familiar with Global Clinical Data Interchange Standards Consortium (CDISC).
Understand clinical data flow . Experience in NDA submission is desired.
Experience in SDTM and / or ADaM specification and programming.
Experience in TFL programming.
Education
Bachelor’s degree or higher in Statistics, Mathematics, or Scientific Discipline
About US Tech Solutions US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit
www.ustechsolutions.com
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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Remote
Job Description
Under the supervision of the Head of Statistical Programming, the Contractor Statistical Programmer will be assigned to work on a TA / Study at Client. The contractor will participate in the oversight, creation, maintenance and finalization of clinical study datasets / TFL for Client development programs, and ensure all clinical datasets perform the analysis defined by SAP and meet the standards required for regulatory submissions for all INDs and NDAs / MAAs
Responsibilities
Responsible for Statistical Programming activities, including analyzing, integrating and reporting of clinical trial data in order to produce quality and timely deliverables.
Performs data analysis using primarily the SAS programming language for the summary and interpretation of clinical trial data.
Provide statistical programming support to generate derived analysis data sets, tables, listings, and figures for Clinical Study Reports, regulatory submissions, annual IND safety update reports and Integrated summaries (ISS / ISE).
Creation / QC of CDISC SDTM and ADaM files, SAS export files and Define.xml use for Electronic Submission from the data received in non-standard form from various sources.
Interact with Statisticians, Programmers and other members of the clinical team, perform ad hoc analysis and generate outputs according to the requirements.
Review and comment on CRFs, annotated CRFs, Data Management Plan, Data validation plan, edit check specifications and study related documents.
Participate in operations meetings and address issues that may influence statistical programming and data management.
Work with CRO statisticians, statistical programmers and review / QC their work / deliveries.
Experience
5+ years’ programming experience in pharmaceutical / biotech / CRO environment in drug discovery / clinical trials / drug development
Experience in working with multidisciplinary groups (internal & external), flexibility, adaptability and ability skills to work within a matrix environment.
Skills
Proficiency in statistical programming package(s), SAS is required ; R or other packages are desired.
Familiar with Global Clinical Data Interchange Standards Consortium (CDISC).
Understand clinical data flow . Experience in NDA submission is desired.
Experience in SDTM and / or ADaM specification and programming.
Experience in TFL programming.
Education
Bachelor’s degree or higher in Statistics, Mathematics, or Scientific Discipline
About US Tech Solutions US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit
www.ustechsolutions.com
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
#J-18808-Ljbffr