Kronos Programmer jobs in the Biotech, R&D, Science category

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work. The Sr. Statistical Programmer will be responsible for technical implementations and data related reporting and product development activities. The p...
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Clinical Data Programmer III - Contract The Clinical Data Programmer will be responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables. Additional responsibilities include quality control of junior programmer deliverables and assisting with project management activities. Overview of the role: Recognize, exemplify and adhere to ICON’s val...
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Clinical Data Programmer III - Contract The Clinical Data Programmer will be responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables. Additional responsibilities include quality control of junior programmer deliverables and assisting with project management activities. Overview of the role: Recognize, exemplify and adhere to ICON’s val...
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Clinical Data Programmer III - Contract The Clinical Data Programmer will be responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables. Additional responsibilities include quality control of junior programmer deliverables and assisting with project management activities. Overview of the role: Recognize, exemplify and adhere to ICON’s val...
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ALEXION PHARMACEUTICALS POSITION SUMMARY Title: Senior Statistical Programmer Reports to: Senior Manager, Statistical Programming Location: Cambridge, MA Company Description Alexion Pharmaceuticals, Inc. is a biopharmaceutical company working to develop and deliver life-changing drug therapies for patients with serious and life-threatening medical conditions. Alexion is engaged in the discovery, d...
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Title: Senior Clinical Programmer (3 Openings) Reports to: Senior Manager, Clinical Programming Location: Cheshire, CT and Cambridge, MA Position Summary The SeniorClinical Programmer will be a primary resource for the development and validation of programs which create and transfer data across multiple data management systems conforming to Alexion and SDTM standards. Additionally, he/she will be ...
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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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This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
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Accelerate your career….Aptiv Solutions…. Accelerating the Possibilities Discover Aptiv Solutions. We’re focused on changing the way that biopharmaceutical and medical device companies develop their products. Join the team that is leading the industry acceptance of adaptive clinical trials – we are the only CRO to both design and execute adaptive trials. Join the market leader in medical device de...
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This is a home based opportunity anywhere in North America. The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improve...
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The Statistical Programmer is responsible for providing significant programming support to the statisticians as part of the contribution towards the completion of statistical analyses (tables, listings and figures) and reporting of results of clinical studies. It includes Safety, Immunogenicity and Efficacy Analysis. In addition, other ad hoc analysis may have to be performed, based on the need, s...
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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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This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
full job description

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
full job description

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
full job description

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
full job description

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
full job description

Clinical Data Programmer III The Clinical Data Programmer will be responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables. Additional responsibilities include quality control of junior programmer deliverables and assisting with project management activities. Overview of the role: Recognize, exemplify and adhere to ICON’s values which c...
full job description

Clinical Data Programmer III The Clinical Data Programmer will be responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables. Additional responsibilities include quality control of junior programmer deliverables and assisting with project management activities. Overview of the role: Recognize, exemplify and adhere to ICON’s values which c...
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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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. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in Bridgewater, NJ RESPONSIBILITIES: Knowledge of FDA regulations (21 CFR part 11) and guidelines in new drug development and application process re...
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This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
full job description

. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in Bridgewater, NJ RESPONSIBILITIES: Knowledge of FDA regulations (21 CFR part 11) and guidelines in new drug development and application process re...
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