Vertex Pharmaceuticals Incorporated
Senior Statistical Programmer II
Vertex Pharmaceuticals Incorporated, Boston, Massachusetts, us, 02298
Employer:
Vertex Pharmaceuticals Incorporated
Job Title:
Senior Statistical Programmer II
Location:
50 Northern Ave., Boston, Massachusetts, 02110
Openings:
1
Duties:
Codes complex SAS programs (including Macro language, SAS/STAT and SAS/GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDDSC SDTM format; consistently meeting objectives of the study.
Performs quality control checks of SAS code and output produced by other Statistical Programmers.
Demonstrates proficient knowledge of clinical development and medical data.
Solves clinical trial reporting problems and has a proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately with limited supervision.
Creates CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications.
Works with all types of coding dictionaries (MedDRA and WHODD) commonly used by the pharmaceutical industry.
Works in a team environment providing technical leadership and solving clinical trial reporting problems within budget and customary timeline constraints while assuring high quality standards.
Telecommuting permitted.
Requirements:
Employer will accept a Bachelor's degree, or foreign equivalent, in Computer Science, Biostatistics, Statistics, Data Science, Engineering, Biology, Pharmacy or a related field, and 5 years of experience in the job offered or in a Senior Statistical Programmer II‑related occupation.
Alternatively, employer will accept a Master's degree, or foreign equivalent, in Computer Science, Biostatistics, Statistics, Data Science, Engineering, Biology, Pharmacy or a related field and 2 years of experience in the job offered or in a Senior Statistical Programmer II‑related occupation.
Position requires demonstrable experience in the following:
Writing SAS programs using SAS/BASE, SAS/MACRO, SAS/GRAPH, SAS/STAT, and SAS/SQL to map raw clinical data to CDISC compliant datasets and create tables, figures, and listings reporting results of clinical trials for investigational medications;
Knowledge on Metadata Submission Guidelines (MSG V2.0) and annotate CRF with SDTM variables;
Knowledge on generation of define.xml 2.1;
Perform quality control on vendor deliverables;
Review CRF design specifications, edit check specifications, manual data review specifications, and vendor data transfer specifications as study statistical programmer;
Knowledge on Clinical Study Data Reviewer's Guide (cSDRG) and Analysis Data Reviewer's Guide (ADRG) documents; and
Reviewing Statistical Analysis Plan.
Rate of Pay:
$124,600.00 - $186,900.00
Contact:
Send Resume to
futuretalent@vrtx.com . Reference 12140.759. EOE.
Application Assistance:
ApplicationAssistance@vrtx.com
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E‑Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
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Vertex Pharmaceuticals Incorporated
Job Title:
Senior Statistical Programmer II
Location:
50 Northern Ave., Boston, Massachusetts, 02110
Openings:
1
Duties:
Codes complex SAS programs (including Macro language, SAS/STAT and SAS/GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDDSC SDTM format; consistently meeting objectives of the study.
Performs quality control checks of SAS code and output produced by other Statistical Programmers.
Demonstrates proficient knowledge of clinical development and medical data.
Solves clinical trial reporting problems and has a proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately with limited supervision.
Creates CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications.
Works with all types of coding dictionaries (MedDRA and WHODD) commonly used by the pharmaceutical industry.
Works in a team environment providing technical leadership and solving clinical trial reporting problems within budget and customary timeline constraints while assuring high quality standards.
Telecommuting permitted.
Requirements:
Employer will accept a Bachelor's degree, or foreign equivalent, in Computer Science, Biostatistics, Statistics, Data Science, Engineering, Biology, Pharmacy or a related field, and 5 years of experience in the job offered or in a Senior Statistical Programmer II‑related occupation.
Alternatively, employer will accept a Master's degree, or foreign equivalent, in Computer Science, Biostatistics, Statistics, Data Science, Engineering, Biology, Pharmacy or a related field and 2 years of experience in the job offered or in a Senior Statistical Programmer II‑related occupation.
Position requires demonstrable experience in the following:
Writing SAS programs using SAS/BASE, SAS/MACRO, SAS/GRAPH, SAS/STAT, and SAS/SQL to map raw clinical data to CDISC compliant datasets and create tables, figures, and listings reporting results of clinical trials for investigational medications;
Knowledge on Metadata Submission Guidelines (MSG V2.0) and annotate CRF with SDTM variables;
Knowledge on generation of define.xml 2.1;
Perform quality control on vendor deliverables;
Review CRF design specifications, edit check specifications, manual data review specifications, and vendor data transfer specifications as study statistical programmer;
Knowledge on Clinical Study Data Reviewer's Guide (cSDRG) and Analysis Data Reviewer's Guide (ADRG) documents; and
Reviewing Statistical Analysis Plan.
Rate of Pay:
$124,600.00 - $186,900.00
Contact:
Send Resume to
futuretalent@vrtx.com . Reference 12140.759. EOE.
Application Assistance:
ApplicationAssistance@vrtx.com
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E‑Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
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