Senior Clinical Programmer at Eisai in Woodcliff Lake, New Jersey

Job Description:

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

Senior Clinical Programmer sought by pharmaceutical company in Woodcliff Lake, NJ. Responsible 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 documentation. Design 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. 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. Requires: Bachelor's degree in Pharmacology, Pharmacology and Toxicology, Biological Science, or closely related life science discipline plus 3 years of relevant pharmaceutical industry SAS programming experience in CRO environment in the job offered or as Senior SAS Programmer Analyst/SAS Programmer. Also requires 3 years of experience with the following (which may have been obtained concurrently): SAS programming experience; clinical trial study/research management; Using SAS/Base, SAS Macros, SAS/Graph, and SAS/SQL; writing SAS tools and developing generic SAS programs for clinical studies; Clinical trial standards such as CDISC and SDTM; MedDRA, WHODRUG; Handling external data, such as lab data, PK, Tumor, Biomarker, and Imaging; Using relational databases such as ORACLE, EDC system, and InForm. Send resumes to Human Resources/KL, Job Code: R835, Eisai, Inc. 100 Tice Boulevard, Woodcliff Lake, NJ 07677.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

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