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Sr, SAS Programming Analyst

Integrated Resources, Inc

Woodcliff Lake, New Jersey

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Analysis Skills, Biomarkers, Case Report Form (CRF), Clinical Data, Clinical Data Interchange Standards Consortium (CDISC), Clinical Practices/Protocols, Clinical Research, Clinical Trial, Computer Programming, Computer Science, Data Management, Data Mapping, Data Sets, Data Structures, Documentation, Electrocardiogram, Electronic Data Capture (EDC), GCP (Good Clinical Practices), Information Technology & Information Systems, Medical Dictionary for Regulatory Activities (MedDRA), Microsoft Windows Operating System, Oncology, Oracle, Organizational Skills, Problem Solving Skills, Project/Program Management, Regulatory Submissions, Rehabilitation Nursing, Relational Databases (RDBMS), SQL (Structured Query Language), Software Development Lifecycle (SDLC), Standard Operating Procedures (SOP), Statistical Analysis System (SAS), Statistics, Team Player, Test Plan/Schedule, Time Management, Unix Operating Systems, XML (EXtensible Markup Language)
LOCATION
Woodcliff Lake, New Jersey
POSTED
1 day ago
Sr, SAS Programming AnalystIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionSr SAS Programmer Analyst - SDTMResponsible for SDTM data creation and delivery for oncology studies.Prepare SDTM Mapping specification following company standards.Create or participate in SDTM annotation for CRFs/eCRFs for oncology trials.Develop programs to create SDTM datasets and Define.xml for statistical analysis, tables & listings, and regulatory submissions.Perform Open CDISC validation, coordinate to resolve issues, prepare associated documentationDesign and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.Ensure all programming activities and processes performed are conducted according to standard operating procedures, good programming practices, and GCP guidelines.Strong problem-solving skills;Able to work independently and as a team player; Good organizational, time management, and project management skills ;Capable of communicating technical conceptsGood understanding of system development life cycles, GCP, and related Regulatory guidelines.Should be able to manage the assigned projects independently with minimum supervision.QualificationsBS or MS in Computer Science or related field;5-7 years of strong experience in programming with clinical trial data and developing programs, testing, and documentation;Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SQL;Extensive experience of handling SDTM mapping, related data structures, and programming to create SDTM data sets;Extensive experience in SDTM validation using OpenCDisc.Good knowledge in developing Define.xml and its validation.Extensive experience of handling external data, e.g., laboratory data, PK, ECG, Biomarker, Imaging, etc.Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG;Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus;Knowledge of using JReview/IReview is a plus;Best RegardsMohit GargIntegrated resources Inc | Team Recruitment | 732-429-1634

About the Company

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Integrated Resources, Inc