New job Clinical SAS Programmer - CDISC, ADaM - Jersey City, NJ

LinkedIn Following

Group: Job Openings, Job Leads and Job Connections! Subject: Clinical SAS Programmer - CDISC, ADaM - Jersey City, NJ Alex Lawless posted a job: Clinical SAS Programmer - CDISC, ADaM - Jersey City, NJ "Clinical SAS Programmer with strong ADaM experience required for a thriving pharmaceutical firm based in Jersey City, NJ. Our client is looking for a candidate who will act as a senior member of the SAS Clinical Programming team and ensure that the delivery of submission datasets that are compliant with industry standards (e.g., CDISC SDTM, ADaM, etc.), development of internal procedures for submission dataset preparation, planning data standards implementation strategies. This is a hands-on lead role where you will have the opportunity to manage teams across important business projects. Major responsibilities will include: • Acting as a project leader role by coordinating project team(s) and study team(s) involving other members of Statistical Programming. • Acting as a primary statistical programmer on all assigned studies, integrated summaries, and responses to requests from regulatory authorities. • Performing the role of validation programmer on all assigned studies, assigned integrated summaries, and responses to requests from regulatory authorities. • Creating data definition tables for all ADaM and derived data sets for all assigned studies and integrated summaries. • Creating data mappings, ADaM and derived data sets, and data definition tables for all assigned partner studies. • Reviewing statistical analysis plans for all assigned studies and integrated summaries and provides comments to study biostatistician. • Reviewing annotated case report forms and provides comments to study designer. Desired Skills & Experience For this role you will need at least 8 years of working as a SAS Programmer within clinical trial data including 2 years of implementing CDISC AdAM. You should also have at least 2 years project lead experience. You must be able to demonstrate clinical programming principles as well as SAS and have sound knowledge of CDISC submission data principle. You must have a Bachelor’s degree in Life Sciences or related field or a similar combination of education and experience is required. You must also have previous experience in pharmaceuticals. On offer is a salary of $90-110K basic + bonus + stock options + benefits. To apply, send your resume to alex.lawless@hays.com"

Go see this job post »

Don't want to get activity notifications: Change your following people settings » Learn more about following people's activity LinkedIn values your privacy. At no time has LinkedIn made your email address available to any other LinkedIn user without your permission. ©2011, LinkedIn Corporation.