Average salary: $109,428 /yearly
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- ...the electronic regulatory submission. Ensure that all deliverables are completed on time and of high quality. Represent the Clinical Programming function at cross-functional meetings. May support EDC development and visualization tools (PowerBI). Requirements...SuggestedWork experience placement
Katalyst HealthCares & Life Sciences
Princeton, NJ2 days ago - ...level documentation • Example outputs and sample displays • Integrated Case Report Forms (iCRFs) • Reviewer documentation: • Clinical Study Reviewer's Guide (cSDRG) • ADaM Reviewer's Guide (aDRG) • Variable derivation documentation and codelist mappings •...SuggestedRemote work
Insight Global
United States1 day ago - ...using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects. Produces and delivers CDISC and regulatory... ...validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. Programs quality...Suggested
Katalyst HealthCares & Life Sciences
Austin, TX4 days ago - ...Responsibilities: Develop and maintain SAS programs to import, clean, and validate clinical trial data. Use R for data manipulation, analysis, and visualization. Perform statistical analyses in accordance with study protocols and analysis plans. Generate...Suggested
Katalyst Healthcares and Life Sciences
Addison, TX1 day ago - ...Wirkstoffforschung (w/m/d) Mathematiker*in / Bioinformatiker*in (m/w/d) Senior Statistiker*in klinische Studien Facharzt für Endokrinologie als Clinical scientist (m/w/d) Münster, North Rhine-Westphalia, Germany Be an early applicant 3 days ago Clinician Scientist / Facharzt fü...SuggestedRemote work
Immatics
New Bremen, OH4 hours ago - A Clinical Programmer will support the design, development, and validation of clinical trial databases. In this role, you will build and test study databases using platforms such as Medidata Rave or OmniComm TrialMaster, program validation checks, and ensure all data structures...SuggestedWork from home
$143k - $169k
...Senior Programmer For Data Validation The Senior Programmer for Data Validation supports cross-functional teams such as Statistics,... ...Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid,...SuggestedWork at officeRelocation packageSeqirus
King of Prussia, PA12 hours ago- ...Responsibilities & Requirements: ~ Provide statistical programming support for clinical trial data reporting under the general guidance of a biostatistician. ~ Develop SAS programs that generate tables, listings and figures and derived datasets that summarize...Suggested
Katalyst Healthcares and Life Sciences
Great Neck, NY1 day ago - A clinical trial consultancy in Covington, Kentucky, seeks a Clinical Programmer to design and validate clinical trial databases. You'll build databases using Medidata Rave or OmniComm TrialMaster and perform user acceptance testing. The ideal candidate has a Bachelor'...Suggested
- ...Sr. Statistical Programmer The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials. This role is key to implementing programming standards and supporting the standardization...SuggestedInterim role
Katalyst HealthCares & Life Sciences
Santa Clara, CA2 days ago $79.5k - $169.4k
...Clinical Study Build Programmer - eCOA 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 employees around the world work to discover and bring life-...SuggestedFull timeFlexible hoursEli Lilly
Indianapolis, IN4 hours ago- ...Job Title Perform data manipulation, analysis and reporting of primarily clinical trial data. Create SDTM data sets. Create analysis data sets. Program and generate tables, listings and graphs (TLGs). Validate and document SAS programs and output. Fulfil...Suggested
Katalyst HealthCares & Life Sciences
Baltimore, MD5 days ago - (Senior) Clinical Statistical Programmer – SAS* Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This...SuggestedPermanent employmentFull timeSummer workImmediate startRemote workRelocation package
Immatics
New Bremen, OH4 hours ago - ...Responsibilities Programming and Development: Write and maintain code for clinical trial data processes, including data extraction,... ...Training and Mentorship: Provide guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating...SuggestedWork experience placement
$88.3k - $220.9k
Senior Clinical Programmer page is loaded## Senior Clinical Programmerlocations: Durham, North Carolina, United States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1539388This Clinical Programmer role at IQVIA supports Risk‐Based Quality Management...SuggestedFull timePart timeImmediate startWorldwide- A global provider of clinical research services is seeking a Senior Clinical Programmer in Durham, North Carolina. This role focuses on developing Key Risk Indicators and Quality Tolerance Limits to support risk management in clinical trials. Key responsibilities include...
- ...A company is looking for a Clinical R Programmer Consultant to join their team. Key Responsibilities Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards Support TLF (Tables, Listings, Figures) generation in R or SAS as needed Collaborate...Remote work
Virtual Vocations Inc
United States4 hours ago $140k - $198k
...multiple diseases. Our robust pipeline currently includes four clinical assets spanning all phases of development, with novel... ...seeking a hands-on strategic Senior Manager, Clinical Statistical Programmer, reporting to our Director of Biostatistics. The ideal candidate...Summer workWork at officeFlexible hoursCompass Therapeutics LLC
Boston, MA4 days ago- Cytel in Boston is seeking a Clinical Programmer to manage and maintain clinical trial data processes. The ideal candidate will have 4-6 years of experience in clinical programming and proficiency in languages like SAS, R, and SQL. Responsibilities include coding, data...
- A global healthcare leader based in Indianapolis is seeking an Advisor, Clinical Study Build Programmer to contribute to clinical trial design and execution. This role involves developing robust study databases and ensuring quality and timelines for clinical projects. Candidates...
- Join to apply for the Clinical SAS Programmer role at Katalyst CRO 3 days ago Be among the first 25 applicants Join to apply for the Clinical SAS Programmer role at Katalyst CRO Get AI-powered advice on this job and more exclusive features. Responsibilities Engage...Contract work
$85k - $95k
The Cardiovascular Research Foundation is looking for a SAS Statistical Programmer in New York, NY. This full-time role involves developing and validating SAS programs for clinical trial data analysis, collaborating with study teams, and ensuring regulatory compliance....Full timeFlexible hours- Cytel is seeking a clinical programmer in Denver, Colorado, to manage and develop clinical trial data processes. The candidate should have 4-6 years of experience and proficiency in programming languages like SAS, R, and SQL. Responsibilities include ensuring data accuracy...
- Cytel in Indianapolis is seeking an experienced clinical programmer to manage programming for clinical trial data processes. Responsibilities include coding, data quality assurance, and collaboration with clinical data teams. Ideal candidates will have 4-6 years of experience...
- Cytel is seeking a Clinical Programmer in Oklahoma City to write and maintain clinical trial data processes. The ideal candidate will have 4-6 years of experience, proficiency in SAS, R, and SQL, and a Bachelor's degree in a relevant field. Responsibilities include data...
- Cytel in Annapolis, Maryland, is seeking a Clinical Programmer with 4-6 years of experience in clinical programming. Responsibilities include writing and maintaining code for clinical trial data, ensuring data quality, and collaborating with clinical data managers and other...
- Cytel in Nashville, TN is looking for a Clinical Programmer with 4-6 years of experience in clinical programming. The successful candidate will write and maintain code, ensure the timely delivery of clinical trial data, and collaborate with clinical data managers and statisticians...
- Cytel is seeking a skilled Clinical Programmer in Austin, Texas to manage clinical trial data processes. The ideal candidate will have 4-6 years of experience in clinical programming, proficiency in SAS, R, and SQL, and strong knowledge of data structures and regulatory...
- A leading biotechnology firm is seeking a Principal Statistical Programmer in Cambridge, MA, to provide programming support for clinical studies. This role involves leadership in data processing, validation of submissions, and collaboration with a multidisciplinary team...
- Katalyst HealthCares & Life Sciences in Chicago, Illinois is looking for a Statistical Programmer. The role involves designing and coding SAS programs for clinical projects and ensuring compliance with CDISC and regulatory standards. Candidates should have an MS or BS...
