Average salary: $109,428 /yearly
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- ...review of 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
- ...A Massachusetts-based pharma company is actively seeking a new Clinical Programmer to join its team. The role offers a dynamic work environment with opportunities for innovation in the healthcare industry. Responsibilities: Developing and validating SAS programs...Suggested
- A specialized staffing agency is seeking a Clinical Programmer to work remotely on a client project. The ideal candidate should have significant expertise in Medidata EDC and C# programming, accompanied by years of experience in clinical research database management. Responsibilities...SuggestedRemote work
- ...Syneos Health is seeking a Clinical Programmer II to join our Clinical Solutions team. You will design, write, validate, and maintain software to meet study specifications, supporting annotated CRFs, databases, and reports. You will lead programming activities on multiple...Suggested
- ...Working remotely, the Clinical Programmer will develop, configure, and quality-check data integrations and exports, troubleshoot data issues, and contribute to process improvements within the Data Management team. Key responsibilities Review and apply data mappings for...SuggestedRemote work
- ...Clinical Programmer Clinical Ink is seeking a Clinical Programmer to join our Data Management team based remotely across the United States! This individual will develop, configure, and quality-check data integrations, exports, custom reports, and database scripts to...SuggestedRemote work
- ...a flexible, part-time, remote engagement evaluating AI-generated healthcare content for accuracy and quality. You will apply real clinical expertise to ensure reliable guidance. Contribute by reviewing material, answering domain questions with clear feedback, and suggesting...SuggestedPart timeRemote work10 hours per weekFlexible hours
- ...experts where they can learn from each other and solve the world’s most complex client challenges.You are:An experienced Epic Certified Clinical Data Model ConsultantThe Work:Depending on the client engagement, the Epic Clinical Data Model Consultant will be responsible for...SuggestedFull timeLive inWork at officeLocal areaImmediate start3 days per week
- ...using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) 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 checks...Suggested
- ...ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all... ...data sets, tables, figures, and listings. Strong level SAS programmer with experience in delivering complex programming assignments,...SuggestedFor contractors
- Job-ID31508345Reference25-04461 Summary: As a Clinical SAS Programmer, you will be responsible for attending multi-disciplinary team meetings to represent the programming function. You will create or review and approve programming plans at study and project levels, providing...SuggestedFor contractors
- Job-ID31607148Reference25-04636 Responsibilities: 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...SuggestedInterim role
- ...staffing company in the United States is seeking a skilled Biostatistician. The role involves providing statistical expertise for clinical trial data analysis and supporting multidisciplinary teams. Responsibilities include managing statistical tasks, contributing to study...Suggested
- ...datasets, and reporting outputs (tables, listings, and figures) for clinical trials in alignment with project requirements and regulatory... ...mentorship and technical leadership to junior statistical programmers by conducting code reviews, sharing best practices, and contributing...Suggested
- ...Heartflow is seeking an Associate Clinical SAS Programmer/Junior Statistician to transform raw clinical trial data into analysis-ready datasets and outputs for submissions, publications, and conferences. Remote with a preference for proximity to the San Francisco office...SuggestedWork at officeRemote work
- ...A leading clinical research organization in California is seeking a skilled Clinical Statistical Programmer. The role involves writing specifications for clinical data, developing algorithms, and producing data listings and summary tables using SAS software. Candidates...
- ...Downtown Boulder Partnership is seeking an experienced SAS Programmer in Indianapolis, Indiana. The ideal candidate will have a minimum... ...manipulation, analysis, and generating comprehensive reports of clinical trial data. Proficiency in using SAS software is essential for...
- ...A leading clinical research organization located in Basking Ridge, NJ is looking for a Manager for Clinical Data Standards. The role involves developing and sustaining global clinical data standards crucial for quality submissions. This manager will work with diverse...Work at office
- ...performing User Acceptance Testing (UAT) Responsible to perform, supervise and manage day-to-day activities associated with receipt of clinical (CRF and non CRF) and operational (when relevant) data in accordance with study timelines Responsible to perform data handling...Work experience placementLocal area
$60k - $70k
Position: Clinical Applications Programmer IISalary Range: $60,000-70,000Location: Baltimore, MDAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over...Contract workTemporary workWorldwideFlexible hours- ...continually foster teamwork. Responsibilities: The SAS Programmer is responsible for developing and executing biostatistical (SAS... ...related programs, processing data from various sources to support clinical and pharmaceutical projects and will include defining...Contract workWork experience placementRelocationShift work
$155k - $212k
...member of our software engineering team, you will design, build, and scale the services that power Xealth’s EHR integrations and clinical workflows. You’ll apply solid computer science fundamentals to solve complex problems in distributed systems, data modeling, and API...Permanent employmentFull timeHome officeFlexible hours$182.3k - $220k
...lead the patient revolution, come build with us. The Role We're looking for a Frontend Engineer to join the Care Platform Clinical Workflows team at Ro. In this role, you'll design, build, and maintain purpose-built provider flows — the web interfaces...Full timeLocal areaFlexible hours$210k - $270k
...Impact on Our Mission Finding the right care is one of the most important decisions a patient can make. As a Staff Engineer on the Clinical Fit team, you'll play a critical role in helping patients connect with the providers, specialists, and care pathways that best...Remote workFlexible hours- ...capacity of the Statistical Programming group At least 6 years of Clinical trials related work experience in SAS programming, analysis... ..., quality) You will work closely in teams led by statistical programmers, statisticians, and drug development consultants, supporting a...Work experience placement
- Job-ID31590458Reference25-04599 Responsibilities: The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research...
- ...disease TA experience is highly preferred.The ideal candidate must be able to communicate effectively within a multi-disciplinary project team to assess priorities and complete assigned tasks on time.Proficient of SAS programming in a regulated clinical research environment.
- ...help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials.• Employ standardized programs where applicable.• Provide input into planning documents such as protocol, validation plan,...Work at officeImmediate startRemote work
- Job-ID31618032Reference25-04664 Responsibilities: Develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD Guarantee quality of statistical output produced by external provider, to program tools to support data...
- ...faculty are leaders in the development of statistical methods for clinical trials and observational studies, studies on the environment,... ...in these programs. Our team invites applications for a Programmer position in the National Studies on Air Pollution and Health group...Work experience placementWorldwide


