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Clinical Programmer Jobs

59 jobs

Overview Programming Lead/Sr. Programming lead is responsible for data definition, processing, data integration and reporting for all clinical trials to ensure all databases meet business objectives of database lock. Secondary function will be to generate database specifications where needed and work with vendors to ensure receipt of data in Teva data standard format. This position is also respo...
Our client has multiple openings for (WORK FROM HOME) Clinical SAS Programmers (Senior or Principle level). The Clinical Programmer is responsible for accessing and assembling clinical data from a variety of sources, converting the data to tabulation datasets and creating derived datasets following industry and client specifications, and generating tables, figures and listings to support analysis....
My client, an elite Pharmaceutical Company, located in Berkeley Heights, NJ is looking to add a Clinical Programmer to their expanding Data Management team. This is an initial 12 month contract with favorable chance of permanent conversion upon completion. Rate is based on experience but could range from $60 - $75 per hour. Responsibilities will include, but are not limited to: 1. Clinical trial...
Hi there! New Contract Opportunity Programmer, Systems and Applications Support Major Biotech Company 6 Months Contract Berkeley Heights NJ 07922 Programmer, Systems and Applications Support Responsibilities: ¨ Write and debug SAS programs/macros in Linux environment. ¨ Participate, manage and perform clinical trial data migration activities from Windows to Linux. Including writing and ex...
TechData is looking for Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting, Clinical Programmer in San Diego , L.A., CA.Please see below requirements and send your resume to: *****. TechData is a leading provider for temporary and permanent positions in the pharmaceutical industry. TechData offers the most competitive pay rate and benefits in ...
1. Provide programming expertise and technical for a Phase I-IV Data Management Technical Support team. 2. Develop and validate study dataset specifications against sponsor libraries and vendor deliverables, CDISC/SDTM review of vendor deliverables, programming support of tools that assist with Data Management activities. 3. Knowledge and experience developing study dataset specifications 4. Ab...
• Review protocols for proper data capture including case report form design • Assist Data Manager on development of eCRF specifications and review according to the protocol • Maintain in-house trials which could include (develop programming, testing and maintaining clinical trial databases) in accordance with company standards • Review computer validation/edit checks if applicable • Developin...
Responsibilities: Statistical Analysis Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans. Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created. Collaborate with data mana...
About Pfizer A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged...
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism...
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism...
Clinical Programmer II - Spotfire - (16002889) Description Summary: Leads, manages, and supports project deliverables and timelines. Designs, writes, validates, and maintains software to meet specifications. Specifies, develops, and validates applications supporting data capture and processing. Essential Functions: Utilizes primary development tools including Oracle RDC, Oracle Inform, Medida...
Description: CLINICAL PROGRAMMER Global leader in pharmaceutical development is seeking an accomplished clinical programmer to join their team Responsibilities will include, but are not limited to: 1. Clinical trial databases: • Review synopsis and/or protocol and provide Data Manager with comments for the Synopsis Review Committee (SRC) meeting • Review protocols for proper data capture incl...
Job Description DescriptionSummary: Leads, manages, and supports project deliverables and timelines. Designs, writes, validates, and maintains software to meet specifications. Specifies, develops, and validates applications supporting data capture and processing. Essential Functions: Utilizes primary development tools including Oracle RDC, Oracle Inform, Medidata Rave, Omnicomm TrialMaster, SA...
About Pfizer A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged...
Job Description: *Please note that this a 6 month contract assignment. Candidates cannot start an assignment until background check and drug test is completed* Responsibilities:Individual will serve as a lead SAS® programmer to provide high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders. The individual will gather and interpr...
Company Description Our company is a global biotechnology company that aims to discover, develop and commercialize innovative medicines so people with serious diseases can lead better lives. Founded in MA. Our company today has research and development sites and commercial offices in the United States, Europe, Canada and Australia. For four years in a row, Science magazine has named our company o...
Description Newly combined with Baxalta, Shire is now the leadingglobal biotechnology company focused on serving people affected by rarediseases and highly specialized conditions. These diseases are oftenmisunderstood, undiagnosed and life-threatening. Our 22,000 employees come towork every day with a shared mission: to develop and deliver breakthroughtherapies for the hundreds of millions of peo...
Newly combined with Baxalta, Shire is now the leading global biotechnology company focused on serving people affected by rare diseases and highly specialized conditions. These diseases are often misunderstood, undiagnosed and life-threatening. Our 22,000 employees come to work every day with a shared mission: to develop and deliver breakthrough therapies for the hundreds of millions of people...
Company Description Our Profession is our Passion! We at RangTechnologies specialize in planning, implementing, managing, and staffing InformationTechnology Solutions and Services. Our goal is to help our clients define their investments in technology, optimize processes that bring fast-track success, and deliver business-critical applications to improve performance. We value diversity. We operat...