Clinical sas programmer jobs in the Biotech, R&D, Science category

If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International has one of the largest global footprints ...
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. Adecco Engineering and Technical has an immediate long term contract job opportunity for a Clinical SAS Programmer in the Kansas City Metropolitan Area. To be considered, candidates must have the ability to work in a quiet professional environment, ability to focus and concentrate for long periods, attention to detail, Microsoft office SAS programming experience using SAS/BASE, SAS/MACRO, SAS/SQ...
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Clinical SAS Programmer Our Pharmaceutical client in the greater New Haven area has an immediate need for 2 contract SAS Programmers for 12 months with the option to be extended. They are seeking candidates who possess 7-9+ years of TLG Programming experience within sponsor and/or CRO environments. The ideal SAS Programmer must have experience creating SAS datasets, generating TLGs/reports, suppor...
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Large CRO is seeking a SAS Programmer for a contract opportunity in RTP, NC. This is a Sr. computer programming position working with clinical trials data. Primary responsibilities include: · Providing clinical data management and biostatistical programming support for various phases of clinical studies. · Activities include importing/exporting data, reformatting raw data to CDISC and/or client sp...
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Large pharmaceutical company in Hopewell, NJ has an immediate need for a contract SAS Programmer. 100% onsite. Role is initially 12 months with the option to be extended. Seeking candidates who possess 9+ years of stateside TLG Programming experience within sponsor and/or CRO environments. Must possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output,...
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Large pharmaceutical company in greater Princeton area has an immediate need for a contract SAS Programmer. Seeking candidates who possess 9+ years of stateside TLG Programming experience within sponsor and/or CRO environments. MS grads preferred, but not required. Must possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output, adhering to CDISC standa...
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TechData is hiring SAS/Stat Programmers (Some can be telecommuting), Biostatistician (Can telecommute), and Architect in Gaithersburg, MD. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitive pay rate and benefits. TechData is the leading supplier in the pharmaceutical consulting industry. Sr. SAS Pr...
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Are you a SAS Programmer, with in-depth knowledge of CDISC and strong experience in the clinical research industry, looking for an opportunity to work on a small team with great internal leadership? We are a small CRO operating in the principal center for the Pharmaceutical Industry in North Carolina. We focus on clinical pharmacology, central nervous system (CNS) and oncology trials, and have a g...
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Senior SAS Programmer Responsible for coordinating and programming of clinical data analyses. Analyzes and evaluates clinical data, recognizes inconsistencies and initiates resolution of data problems. Typically programs using SAS language to support the clinical area. Implements statistical analysis plans; may consult in the design and development of clinical trials, protocols, and case report fo...
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Large pharmaceutical company in Central NJ has an immediate need for a contract based SAS Programmer. Role is approved through year end with the option to be extended. Prefer MS level grads, but will consider BS level candidates. Prospects must possess 5+ years of SAS programming experience within an Outcomes Research or Analytics department within a sponsor or specialty firm. Candidates must have...
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3+ years of Clinical SAS programming experience. Mid Level to Lead Programmer openings available. Experience programming with CDISC Standards. Serve as contact with clients for programming aspects of clinical studies Review shell data displays for consistency and to ensure that all CRF fields are displayed on listings Ensure overall consistency of a project including macro definitions, debugging p...
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TechData is hiring Biostatistician (Some positions can be telecommute), SAS Programmer/Statistical Programmer (Some can be telecommuting), Sr. Clinical Data Manager, Director of Medical Affairs, Informed Consent Specialist, Clinical Scientist, CRS (Clinical Research Scientist), Clinical trial manager/Leader for our pharmaceutical clients in Northern and Central NJ. Please see below requirements an...
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TechData is hiring SAS Programmer (Some positions can be telecommute), clinical Data Analyst, Biostatistician (some can be telecommuting), Clinical Data Manager, Clinical Outsourcing Consultant, Clinical Research Scientist for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData is...
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Contributes to the development of SAS programs in support of clinical data analysis performed by statisticians and clinical groups, including creating data sets to produce data analysis tables and lists. Key Job Responsibilities Key job responsibility Percentage of time spent on performing it The importance rank * Provides analysis programming including generating reports, tables, listings, graphs...
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TechData is hiring Outcome Research Statistician, Biostatistician(Some can be remote), SAS Programmers (Some can be telecommuting), Drug Safety Specialist and Trial Safety Manager, Medical Data Manager,Clinical Data Manager, Document Specialist in Central and Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData...
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TechData is looking for Validation Analyst (6 positions), Sr. Drug Safety Associate, Computer System Quality Assurance, SAS Programmer (Some can be telecommuting), Biostatistician, Sr. Clinical Data Manager for our pharmaceutical clients in SFC, CA. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitiv...
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We are currently seeking a Senior Statistical Programmer! This person can be based in our Princeton, NJ office or work remotely. Responsibilities: The role of the Senior Statistical Programmer is to assist in provisional of Statistical Programming service. This individual will develop and review SAS programs and output for the management and reporting of clinical trial data. They will act as Lead ...
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Clinical Data Programming Analyst - Provide technical assistance as part of a team to develop and maintain clinical systems that meet internal and external clients' needs. Plan and coordinate database design and development for local, regional, or transnational use. Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. Provide technica...
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Job Number: 412447 Statistical Programmer Analyst Position Statistical Programmer Analyst Job Summary/Purpose: Experienced SAS programmer with good knowledge of Drug Safety databases. • Assumes responsibility for the analysis of data from the Drug Safety Database. • Develops, tests, documents, maintains and validates programs written in SQL, PL/SQL and SAS. Primary Job responsibilities: The functi...
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Statistical Programmer - REMOTE! Responsibilities: Provide programming support and assist with statistical reporting procedures per Biometrics Department standard operation procedures Create SAS datasets of clinical data from databases Create safety and efficacy datasets Prepare documentation describing all datasets and variables Perform data checks as needed Requirements for Statistical Programme...
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Research Associate – Statistical Programmer The Health Economics Resource Center (HERC) conducts cutting-edge research to improve the efficiency and value of the U.S. health care system. We invite you to join our group of economists, programmers, and research support staff in fulfilling this mission. More information about our center can be found at http://www.herc.research.va.gov. We are hiring a...
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We are seeking a Senior Statistical Programmer for our Database Programming Group! Responsibilities: •Act as the Lead Programmer for assigned projects. Ensure quality of personal work and the work of the team when acting as a Lead Programmer. •Assume team member responsibilities, including representing Database Programming at internal project team meetings, client meetings and audits. •Provide inp...
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Shall provide statistical programming SAS in the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical. st...
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Shall provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data. Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical. statistical reports and other similar reports. Contribut...
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Job Description Opportunity: Are you a bio-pharmaceutical e-clinical professional or a seasoned clinical trials leader looking for an exciting new opportunity where you’ll get exposure to a variety of projects and activities? One where you’ll be able to see the fruits of your labor directly reflected in the performance and growth of a young and growing organization? If yes, then this position is t...
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