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Senior Clinical Systems Programmer (JReview), Data Operations

Integrated Resources, Inc

Woodcliff Lake, New Jersey

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Clinical Data, Clinical Data Interchange Standards Consortium (CDISC), Clinical Data Management, Clinical Information Systems, Clinical Practices/Protocols, Clinical Support, Clinical Trial, Computer Programming, Customer Support/Service, Data Cleaning, Data Management, Data Structures, Documentation, Electrocardiogram, Electronic Data Capture (EDC), Financial Reporting, GCP (Good Clinical Practices), Medical Dictionary for Regulatory Activities (MedDRA), Metrics, Microsoft Windows Operating System, Oncology, Oracle, Organizational Skills, Relational Databases (RDBMS), Reporting Skills, SQL (Structured Query Language), Software Design, Software Development, Software Development Lifecycle (SDLC), Standard Operating Procedures (SOP), Standards Development, Statements on Auditing Standards (SAS), Statistical Analysis System (SAS), Systems/Internals Programming, Team Player, Time Management, Training/Teaching, Unix Operating Systems
LOCATION
Woodcliff Lake, New Jersey
POSTED
1 day ago
Senior Clinical Systems Programmer (JReview), Data OperationsAccountable for setting up studies & developing standard programs to create reports, listings, graphs, metrics for clinical data management and other areas of clinical for data review and data cleaning to conduct clinical trials in Oncology area within JReview environment. Develop standard programs for patient profiles, standard and ad-hoc reports for data review using JReview & SAS to support the clinical teams. Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities. • Develop standard / ad-hoc JReview /SAS programs to provide complex listings/reports to support Data Management and clinical functions to clean and review data for Oncology trials. • Set up studies in JReview, develop & maintain programs, support users, and provide training for JReview. • Develop programs to provide metrics, graphs, patient profiles and ad-hoc reports for data review to support the clinical teams. • Design and develop macros, applications, and other utilities to expedite programming activities and usage by the Oncology Data Management and other areas of Clinical for data review. • Develop and maintain the programs with proper documentation and testing using departmental standards. • Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming practice.• Strong SAS programming skills in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/AF, SQL; • Strong JReview skills in terms of program development, administration, maintenance, and user support; • Extensive experience of handling external data, e.g., laboratory data, PK, ECG,Tumor, etc.; • Knowledge of developing reporting or other applications using SAS; • Knowledge of data management process; Good understanding of data cleaning process; • 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; • Strong problem-solving skills; • Able to work independently and a team player; Good organizational and time management skills ; • Capable of communicating technical concepts • Good understanding of system development life cycles, GCP, and related Regulatory guidelines.

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Integrated Resources, Inc