Accountable for developing complex macros and programs to create standard reports and listings for clinical data management and other areas of clinical using SAS for data review and data cleaning to conduct clinical trials in Oncology area. Help in creating SAS tools as needed to expedite SAS programming activities.Develop SAS programs to provide complex data review listings/reports to support different functional groups in Oncology area.Program data review checks as necessary to facilitate data cleaning activities.Design standard programs and macros using study metadata.Design and develop SAS macros, applications, and other tools to expedite SAS programming activities to support different areas of Clinical data review.Develop standard SAS utility macros for developing standard programs.Develop and maintain the programs including testing and organizing the SAS datasets, SAS programs and related documentation.Develop SDTM annotated eCRF , Mapping Specifications, SDTM Datasets and Define.xml for Analysis and Regulatory submissions.Perform OpenCDisc validation, coordinate to resolve issues, prepare associated documents including SDRG document.Ensure all programming activities performed following standard operating procedures and good programming practices. Requirements & Experience : Candidate must have at least a Bachelor degree in Science or Technology with a minimum of 7 years SAS programming experience and 3-5 years of relevant industry experience.Strong SAS programming skills required in Windows & UNIX environment with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/SQL.Experience in writing SAS tools, developing generic SAS programs and SDTM packages for clinical studies.Knowledge of working in SAS Grid environment with experience in SAS Enterprise Guide, SAS Data Integration Studio, SAS Studio is a plusGood understanding of relational databases such as ORACLE, Knowledge of the EDC system, InForm, and underlying data structure is desirable.Experience with all clinical phases I, II, III and IV of oncology trails is desirable.Good understanding of Recist, mRecist, irRecist, Rano criteria.Extensive experience in handling external data, such as lab data, PK,Tumor,Biomarker,Imaging etc.Good understanding of standards specific to clinical trials such as CDISC, SDTM, MedDRA, WHODRUG.Good understanding of system development life cycles, GCP, and related regulatory guidelines.Good understanding of Regulatory requirements for submissions to FDA, PMDA and MHRA.Strong problem solving skillsAble to work independently and a team player, good organizational and time management skills.Excellent communication skills & capable of communicating technical conceptsExcellent organizational skills, demonstrated success to multi-task and deliver viable solutions in a fast-paced environment with changing priorities. NOTE: We need someone experienced in writing complex macros and generic programs and related experience.
About Us : Since 2004, Orbis Clinical has been a leading global recruiting partner to the life sciences industry, helping to drive the success of our clients, consultants and employees. Our clients range from venture-backed start-ups to Fortune 500 firms, and we match your skills, experience and career aspirations to find you just the right fit. We have the unique opportunity to make a meaningful impact on the future of healthcare by finding the best minds in life sciences (like yours!), and pairing them with both emerging and established companies who are innovating treatments with a variety of organizations, including: Biotech/Pharmaceutical Medical Device Clinical Research Organizations (CROs) Hospitals, Universities, and Research Sites Government and Academic Institutions
Why Work With Us : Individual dedicated recruiter Access to benefits, including health, vision and 401k Weekly pay Deep networks to connect you with the most up-and-coming, recognized positions in your field
PandoLogic. Category: Technology, Keywords: Clinical Programmer
Tagged as: management
To apply, please visit the following URL:https://www.jobs2careers.com/click.php?jid=4195086c2fcd61eeb82eda6e9&ri=944d41b48b52498aa9c1177c300ab8d0&job_loc=Nutley%2CNJ&q&spl=W8Ufgn0Xa0qH0Ciy%3AECwv1kFD%2B9kTGk9wXmL9Sg%3D%3D%3AFRODKQ0wRqsOuC5OsC0bmct9AbLbryKEZ4ieogjYIQ%3D%3D&encrypt=0&l=New+York%2C+NY→