Hi Partner, *SEND RESUMES TO [email protected]*
Job Role: SAS developer with core banking/marketing side of pharma Location: richmond,VA Duration: 3+ Months Immediate Interview *SEND RESUMES TO [email protected]* Experienced SAS Programmer to assist with analysis of medical products stability/expiration data. Duties: (1) Develop Programs that convert raw SAS datasets to standardardized structure. (2) Develop Programs that produce analysis datasets from raw data or standard data. (3) Program Data Displays (Tables, Listings, Graphs) for inclusion in documents including publications, stat reports, clinical study report and other regulatory documents. (4) Peer review of SAS Programming Code and deliverables (derived data, tables, listings graphs). (5) Participate in project meetings. (6) Prepare documentation on above production programming and validation activities. Experience: Strong programming skills in SAS in a medical products/devices environment. Possess data analysis and problem solving skills; strong written and verbal communication skills. Experience or degree in statistics preferred, but not required. Requirements: Bachelor’s degree plus 3+ years of SAS experience in the medical devices or pharmaceutical industry. Responsibilities: 1) Create tables and listings according to applicable SOPs as well as the project's Data Management Plan (DMP). Develop tables, listings, and reports for Annual IND Safety update, Medical Coding, and any safety/ad-hoc data reviews with minimal guidance. 2) Participate in Case Report Form (CRF) review process to make recommendations from a programming/CDISC perspective. 3) Perform CDISC to CRFs mappings, annotations and create Case Report Tabulations (CRTs) using CDISC SDTM (Study Data Tabulation Model) specifications. 4) Develop and process specifications for multiple data transfers. Manage Data Transfer Agreements (DTAg) and Data Transfer Acceptance (DTAc) forms and work with CROs (Contract Research Organizations), LABs, and technology vendors to resolve any issues. 5) Address ad-hoc programming requests and perform validation tasks. 6) Develop, share, and document innovative programming techniques for data review. 7) Review and validate other programmer’s work. Qualifications: 1) Strong analytical, organizational and excellent communication skills (both verbal and written). Ability to work on a multi-disciplinary team. 2) Exposure/Experience with CDISC Models like SDTM, LAB etc. 3) Programming expertise in SAS. Recent SAS Certifications preferred. 4) Understanding of database concepts. Education/Experience: Bachelor's degree required, Master’s degree preferred. 1+ years of programming experience, preferably using SAS in Clinical R&D in Pharmaceutical/Biotech industry (Sponsor, Contract Research Organization (CRO), or a combination of both) -- Thanks & Regards, *Naveen Krishna* Cloudeeva, Inc. Phone No:732-476-5241 Email: [email protected] *Yahoo IM: reachknk86* -- You received this message because you are subscribed to the Google Groups "Vendors" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/vendors. For more options, visit https://groups.google.com/groups/opt_out.
