Capital OneWashington
As a Capital One Lead Data Engineer, you’ll have the opportunity to be on the forefront of driving a major transformation within Capital One. Utilize programming languages like Java, Scala and Open Source RDBMS and NoSQL databases and Cloud based data warehousing services such as Redshift and Snowfl...
Capital OneWashington
Senior Data Engineer - Principal Associate. As a Capital One Data Engineer, you’ll have the opportunity to be on the forefront of driving a major transformation within Capital One. Utilize programming languages like Java, Scala, Python and Open Source RDBMS and NoSQL databases and Cloud based data w...
Capital OneWashington
Senior Software Engineer, Full Stack. As a Capital One Software Engineer, you’ll have the opportunity to be on the forefront of driving a major transformation within Capital One. At least 4 years of experience in software engineering (Internship experience does not apply).
Share your passion for sta...
Katalyst Healthcares & Life SciencesWashington
Life Cycle and CDISC standards (SDTM & ADaM).
Solid knowledge of other software such as SpotFire, R Shiny etc. is a plus.
BS/MS in Statistics, Math or Scientific Discipline.
Requirements:
Lead clinical studies and integrated analyses and provide...
TTI of USA, Inc.Owings Mills, 37 mi from Washington
The Systems Programmer will be responsible to install, maintain, and upgrade IBM and 3rd Party products in a mainframe z/OS environment using SMP/E and zOSMF. Ability to conduct strong engagements with corporate partners and vendors is essential...
TechWishTysons Corner, 11 mi from Washington
understanding of OAS concepts and lifecycle.
• Knowledgeable with google analytics.
• SEO
Soft skills:
• Experience in an Agile/Scrum software development environment.
• Analysis skills
• Take accountability for delivering results
• Strong communication...
GuidehouseMc Lean (VA), 12 mi from Washington
will include:
• Provide Subject Matter Expertise in regulatory frameworks to the team in interpretation and analysis of data collected under Section 1071, Regulation C, or similar, assisting with translating regulatory requirements into tasks for programmers...
National Security AgencyFort George G Meade, 21 mi from Washington
researchers, programmers, and developers who operate in teams in areas such as software engineering, information technology infrastructure, high performance computing, data science, architectures, computer security, and networking in order to design...
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Clinical SAS programmer
Baltimore | www.resume-library.com |
Responsibilities:
Serves as the primary project team representative, delegating work as appropriate
Generates SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data
Reviews output across programs to ensure consistency
Reviews maintains and approves study documents per standard procedures
Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures
Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting
Participates in the development and/or maintenance of departmental procedures and standards
Requirements:
BS/BA degree in computer science, mathematics, statistics, or related discipline and 5+ years' experience in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph). In addition, you must have at least three years of experience serving in a supervisory or lead capacity.
Experience managing projects OR
Demonstrates strong knowledge with industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
Strong programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar
Strong knowledge of SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Strong knowledge of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems
Strong understanding of relational databases and experience working with complex data systems
Understands key business drivers and uses this understanding to accomplish work
Has strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas
Serves as the primary project team representative, delegating work as appropriate
Generates SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data
Reviews output across programs to ensure consistency
Reviews maintains and approves study documents per standard procedures
Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures
Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting
Participates in the development and/or maintenance of departmental procedures and standards
Requirements:
BS/BA degree in computer science, mathematics, statistics, or related discipline and 5+ years' experience in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph). In addition, you must have at least three years of experience serving in a supervisory or lead capacity.
Experience managing projects OR
Demonstrates strong knowledge with industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
Strong programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar
Strong knowledge of SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Strong knowledge of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems
Strong understanding of relational databases and experience working with complex data systems
Understands key business drivers and uses this understanding to accomplish work
Has strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas
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