SDTM, Clinical SAS Programmer
Creative Solutions Services, LLC
Job Description: Looking for SDTM experts having in-depth knowledge of SAS programming(macro's). Must have 10 yrs of exp in clinical domain. Strong knowledge of SDTM. Create advanced SAS macros, templates, and utilities for efficient data processing. Act as the primary programming point of contact for biostatisticians and study teams. Perform peer review of code and documentation for accuracy and traceability. Review CRF (Case Report Form) annotations and data specifications. Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines. Skill: Extensive programming experience in a clinical trial environment (CRO/Pharma). Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. In-depth knowledge of CDISC standards and regulatory submission requirements. #J-18808-Ljbffr Creative Solutions Services, LLC
- Creative Solutions Services, LLC is seeking a Senior SAS Programmer with 10+ years in the clinical domain to drive SDTM/CDISC workstreams in a CRO/Pharma setting. You will lead complex SAS programming efforts and mentor junior staff. You will develop advanced SAS macros...SAS
$61k - $155k
HCLTech is seeking a skilled SAS Programmer in Montgomery County, North Wales, to design efficient data processing utilities and collaborate... ...The ideal candidate will have 5-7 years of experience in the clinical domain. This position offers a pay range from $61,000 to $155...SAS- ...tables, listings, and figures) for clinical trials in alignment with... ...study data tabulation models (SDTM) in compliance with CDISC standards... ..., maintain, and optimize SAS programs, macros, and templates... ...leadership to junior statistical programmers by conducting code reviews,...SAS
- ...501 Allendale Rd., King of Prussia, PA. Responsibilities Write SAS codes to produce CDISC compliant datasets. Create statistical analysis... ..., abstracts, posters, manuscripts, ad-hoc reports, and other clinical publications. Write QC SAS programs for dataset, tables,...SAS
- ACL Digital in King of Prussia is seeking a SAS Programmer to develop and enhance SAS codes for CDISC compliant datasets. You will produce statistical analysis outputs for clinical publications and write QC SAS programs following departmental procedures. The role involves...SAS
$61k
Key Responsibilities Create advanced SAS macros, templates, and utilities for efficient... .... Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines. Skill Requirements... ...Extensive programming experience in a clinical trial environment (CRO/Pharma). Expertise...SASLocal area- ...internal growth. Job Overview : The Statistical Analytical Programmer plays a key role in turning complex EMR-focused real-world... ...and high-quality study outputs. This person will bring strong SAS programming experience and a practical understanding of observational...SASLocal areaRemote work
- Merck & Co., Inc. is seeking a skilled statistician to support clinical safety evaluations within the BARDS (Biostatistics and Research Decision... ...’s with 3+ years of relevant experience), strong knowledge of SAS and R, and excellent communication to convey results to #J-1880...SAS
- MSD Malaysia is seeking a programming professional to support statistical programming activities for clinical trial data analysis. The role requires developing SAS programs to create and validate analysis datasets for Clinical Study Reports and regulatory submissions....SAS
$117k - $184.2k
...and global human health. The Clinical Safety Statistics (CSS) group... ...Development Statisticians, Statistical Programmers, and others) on the planning... ...processing software such as SAS and R (R-Shiny a plus). Strong... ...CDISC standards, including SDTM and ADaM datasets. Knowledge of...SASFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- ..., we strive to continuously develop new technology and drive process improvement. Position Summary As a CNC Swiss Lathe programmer, you will be responsible for reading and interpreting technical blueprints, inputting the design specifications, adjusting the machine...For contractors
- ...Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better data leads to better decisions in...
- CSL Behring seeks a Senior Programmer to build secure, scalable applications that power pharmaceutical R&D and data management. In this... ...design and implement enterprise software, integrate scientific and clinical systems, and ensure compliance with GxP and data integrity...
- ...Experience with migration to AWS. Cotiviti is a leading solutions and analytics company that leverages unparalleled clinical and financial datasets to deliver deep insight into the performance of the healthcare system. These insights uncover new opportunities...H1bWork at office
- ...Senior Software Engineer We are looking to hire a senior Software Engineer to support CCCR (Cross Claim Clinical Review) as an innovative approach to inpatient clinical reviews, currently available through our Retrospective CCV program. This initiative will extend...
$190.8k - $300.3k
...vaccine projects in Late Development Statistics. Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company... ...knowledge of- statistical and data processing software e.g. SAS and/or R.- Good understanding of worldwide regulatory...SASContract workWork experience placementLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work$190.8k - $300.3k
...vaccine projects in Late Development Statistics. Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our... ...Solid knowledge of statistical and data processing software e.g. SAS and/or R. Good understanding of worldwide regulatory requirements...SASContract workFor contractorsWork experience placementLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work- ...Overview: Cotiviti is a leading solutions and analytics company that leverages unparalleled clinical and financial datasets to deliver deep insight into the performance of the healthcare system. These insights uncover new opportunities for healthcare organizations to...
- AutoCad/Revit Technician and Equipment Programmer Proficient in AutoCAD and/or REVIT architectural Programming manufacturing equipment for modular construction Company PDM Constructors & Durapods Location North Wales, PA Date Posted Jul 2022 Job Type Full-Time Philadelphia...Full timeWork at office
- ...governance, and continuous enhancement of Almac’s Clinical Data Management (CDM) standards, policies,... ...oversight, and internal readiness.CDISC SDTM/ADaM-aligned deliverables, including... ...data analysis and reporting software (e.g., SAS and/or SQL).Strong understanding of...SASTemporary workWorldwide
- ...RPG Programmer Fort Washington, PA (Hybrid) 6+ months Contract Pay Rate: $57 W2/$63 C2C Will need to be on-site from time to time and be on-site for the first few weeks to meet the teams and learn the systems – ideal candidate will be within 1-2 hour drive...Contract workLocal area
- Responsibilities Support statistical programming activities for clinical trial data analysis. Develop SAS programs to create and validate analysis datasets (ADaM... ...plans. Utilizing CDISC standards to create ADaM and SDTM datasets. Designing and developing complex programming...SASFor contractors
$117k - $201.25k
...intelligence, this individual will help establish the semantic foundation required to connect discovery biology, preclinical safety, clinical development, real-world evidence, and post-marketing safety into a unified reasoning framework.The successful candidate will...Full timeLocal areaImmediate start- Are you willing to make a difference?At Kulicke and Soffa, (NASDAQ:KLIC) our engineers make that decision daily. We are an international leading provider of robotic semiconductor packaging and electronic assembly solutions supporting the global automotive, consumer, communications...
- ...providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives...Full timeWork at office
- You are joining a highly skilled and motivated software development team on a mission to develop control software for high precision semiconductor assembly and packaging equipment. Together with your colleagues you are making an impact on the full development cycle of new...Work experience placement
- Job DescriptionAt IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We ...Night shiftDay shiftAfternoon shift
- ...providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives...Full time
$156.9k - $247k
...development, qualification, and validation; and design control and risk management techniques to positively support and influence clinical and commercial inhalation combination product development and launches, including device-platform selection, drug-device interface...Full timeFor contractorsLocal areaWorldwideFlexible hours$117k - $184.2k
...activities for late stage drug/vaccine clinical development projects. This may... ...-quality deliverables.Provide SAS programming support for... ...) dataset specifications and SDTM data to programmatically... ...questions as required.Mentor junior programmers and work with third party...SASFull timePart timeFor contractorsLocal areaRemote workVisa sponsorshipFlexible hours
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