Senior Clinical Database Programmer SAS SDTM

Title: Senior Clinical Database Programmer - SAS, SDTM

Department: Biostatistics Clinical Programming

Location: USA - Massachusetts - Billerica

Employment Type: Full Time

Job Type: RegularCompany Profile:PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:SAS Programmers (Senior Clinical Database Programmers - SAS, SDTM, eClinical, EDC, IVRS, ePRO, CTMS, CDISC)Do you possess cutting edge SAS programming expertise and a keen understanding of clinical trials? Do you have what it takes to be part of a high growth team? Come to an industry leader where you will have the opportunity to function as a subject matter expert working independently to support various programming activities related to clinical systems and/or the applications/systems within eClinical technologies. Liaise with sponsors, Data Operations Leaders, and other functional areas as required. Lead programming teams to successful completion of studies within given timelines and budgets. Join PAREXEL where you will extract clinical trial data from databases, manipulate the data, data map, and create reports, developing a wider knowledge of areas of Clinical Data Management Systems (CDMS), Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), Safety Reporting, SAS, SQL, and other programming language usage.GROWTH:While most companies were busy downsizing, during 2010 PAREXEL opened two new offices and added over 800 employees!PROMOTION:In 2010, more than 1,700 PAREXEL employees received career promotions!!EXPERTISE:PAREXEL's experts, who have experience across a broad range of therapeutic areas, have supported nearly all of the top 50 best-selling drugs that are on the market today.AWARDS:- PAREXEL was named Company of the Year 2010 for the Pharmaceutical Industry in The Eighth Annual International Business Awards, the only global, all-encompassing business awards program honoring great performances in business.- PAREXEL announced that the Company had been included on the 'Best 5'Pharmaceutical' industry sublist 2010 as part of The International Association of Outsourcing Professionals® (IAOP®) annual ranking of The Global Outsourcing 100.- PAREXEL was recognized as a Best 10 Outsourcing Company for the Pharmaceutical Industry as part of the Global Outsourcing 100® 2010, and also received a Scrip Award for Clinical Research Team of the Year.- PAREXEL was recognized as Best Performing CRO 2009 by BioSingapore for its leadership in the Asia/Pacific region, and ranked in the Top 10 among best performing Massachusetts-based public companies in The Boston Globe 100, as well as a Top Employer (ranked by a number of worldwide employees)Keywords: SAS, PL/SQL, CDISC, ODM, SDTM, CDASH, xml, EDC, ePRO, IVRS, CTMS, 21 CFR Part 11, ICH, GCP, Perl, Python, UNIX shells, eClinical, Biostatistics, Data Management, Clinical Database Programming, Records Management, Statistical Analysis and Reporting, Data operations, interactive voice response systems, rave, inform, datalabs, trialworks, clinphone, perceptive informatics, clinical research, clinical trial, clinical trail, clinical study, CRO, pharmaceutical, biotechnology, biotech, medical device

Experience:-Proficient in SAS-Possess experience working on clinical trials-SDTM knowledge is desirable-Strong leadership ability, with specific attention to detail-Business/Operational skills that include customer focus, commitment to quality management and problem solving-Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial