Experience in Accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, ...
Experience in Accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, ...
Clinical SAS Programmer
Chantilly, VA · Remote
The ideal candidate will be responsible for creating and validating SDTM domains and ADaM datasets, developing mapping specifications, and supporting clinical data programming activities with ...
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Clinical SAS Programmer
Chantilly, VA · Remote
The ideal candidate will be responsible for creating and validating SDTM domains and ADaM datasets, developing mapping specifications, and supporting clinical data programming activities with ...
Statistical Programmer II
Tampa, FL · On-site
Performed CDISC Mapping for Ongoing clinical trials and classified data into domains. understanding with CDISC SDTM Implementation Guide v3.1.2/ v3.1.3 and SDTM Model. Proficient in generating ...
New
Statistical Programmer II
Tampa, FL · On-site
Performed CDISC Mapping for Ongoing clinical trials and classified data into domains. understanding with CDISC SDTM Implementation Guide v3.1.2/ v3.1.3 and SDTM Model. Proficient in generating ...
New
Prepare SDTM Mapping specification following company standards. * Create or participate in SDTM annotation for CRFs/eCRFs for oncology trials. * Develop programs to create SDTM datasets and Define ...
Prepare SDTM Mapping specification following company standards. * Create or participate in SDTM annotation for CRFs/eCRFs for oncology trials. * Develop programs to create SDTM datasets and Define ...
Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification and submissions support. About the Role * Independently ...
Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification and submissions support. About the Role * Independently ...
Clinical Trial Biostatistician
Bethesda, MD · On-site
Develop, program, and validate CDISC SDTM datasets from raw clinical data (e.g., demographics, adverse events, labs, vitals, concomitant medications). * Develop, program, and validate CDISC ADaM ...
Clinical Trial Biostatistician
Bethesda, MD · On-site
Develop, program, and validate CDISC SDTM datasets from raw clinical data (e.g., demographics, adverse events, labs, vitals, concomitant medications). * Develop, program, and validate CDISC ADaM ...
Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. * Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently ...
Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. * Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently ...
Develop, program, and validate CDISC SDTM datasets from raw clinical data (e.g., demographics, adverse events, labs, vitals, concomitant medications). * Develop, program, and validate CDISC ADaM ...
Develop, program, and validate CDISC SDTM datasets from raw clinical data (e.g., demographics, adverse events, labs, vitals, concomitant medications). * Develop, program, and validate CDISC ADaM ...
Lead Clinical Programmer
Boston, MA · On-site
This position is responsible for taking a lead role in SAS programming support of centralized specification, production and QC of SDTM datasets for use by Statistical Programming and others, and in ...
Lead Clinical Programmer
Boston, MA · On-site
This position is responsible for taking a lead role in SAS programming support of centralized specification, production and QC of SDTM datasets for use by Statistical Programming and others, and in ...
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Develop SDTM CRF annotations and SDTM specifications, as well as analysis dataset specifications to ensure accurate implementation of SAPs and TLF shells * Perform hands-on programming to create and ...
Develop SDTM CRF annotations and SDTM specifications, as well as analysis dataset specifications to ensure accurate implementation of SAPs and TLF shells * Perform hands-on programming to create and ...
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory requests, publication needs, and ad-hoc analyses. * Manage CROs and contractors, ensuring compliance ...
Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory requests, publication needs, and ad-hoc analyses. * Manage CROs and contractors, ensuring compliance ...
Title: Clinical Programmer 2 - Manager Level (SDTM) Shift Schedule: Morning - US time zone 8 hours/day - preferably East Coast Temp to Perm: Not at this time Core essential: 1. Minimal Bachelor ...
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Title: Clinical Programmer 2 - Manager Level (SDTM) Shift Schedule: Morning - US time zone 8 hours/day - preferably East Coast Temp to Perm: Not at this time Core essential: 1. Minimal Bachelor ...
This position is responsible for taking a lead role in SAS programming support of centralized specification, production and QC of SDTM datasets for use by Statistical Programming and others, and in ...
This position is responsible for taking a lead role in SAS programming support of centralized specification, production and QC of SDTM datasets for use by Statistical Programming and others, and in ...
Prepares SDTM and AdAm Submission packages, including, define.xml, Reviews guide, and annotated eCRF. * Generates and validates Tables, Figures, and listings (LTFs) according to approved ...
Prepares SDTM and AdAm Submission packages, including, define.xml, Reviews guide, and annotated eCRF. * Generates and validates Tables, Figures, and listings (LTFs) according to approved ...
Extensive experience and understanding in SDTM model including transforming raw data files while adhering to CDISC standards from end to end (raw data to eSub); advanced understanding of SDTM model ...
Extensive experience and understanding in SDTM model including transforming raw data files while adhering to CDISC standards from end to end (raw data to eSub); advanced understanding of SDTM model ...
Biostatistician
Western Springs, IL · On-site
Learns the role that SDTM & ADaM plays in the standardization of clinical trials data/CDISC. * Able to prepare specifications for simple analysis data sets (CDISC and CDISC-like) independently or ...
Biostatistician
Western Springs, IL · On-site
Learns the role that SDTM & ADaM plays in the standardization of clinical trials data/CDISC. * Able to prepare specifications for simple analysis data sets (CDISC and CDISC-like) independently or ...
Learns the role that SDTM & ADaM plays in the standardization of clinical trials data/CDISC. * Able to prepare specifications for simple analysis data sets (CDISC and CDISC-like) independently or ...
Learns the role that SDTM & ADaM plays in the standardization of clinical trials data/CDISC. * Able to prepare specifications for simple analysis data sets (CDISC and CDISC-like) independently or ...
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for SDTM datasets. * Following statistical analysis plans and the Analysis Data Model (ADaM ...
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for SDTM datasets. * Following statistical analysis plans and the Analysis Data Model (ADaM ...
Sdtm information
See salary details
$19.23 - $24.78
4% of jobs
$24.78 - $30.33
9% of jobs
$30.33 - $35.88
4% of jobs
$35.88 - $41.43
7% of jobs
$41.78 is the 25th percentile. Wages below this are outliers.
$41.43 - $46.98
9% of jobs
The median wage is $52.53 / hr.
$46.98 - $52.53
17% of jobs
$52.53 - $58.09
7% of jobs
$58.09 - $63.64
14% of jobs
$65.40 is the 75th percentile. Wages above this are outliers.
$63.64 - $69.19
12% of jobs
$69.19 - $74.74
10% of jobs
$74.74 - $80.29
7% of jobs
$19
$54
$80
How much do sdtm jobs pay per hour?
What is an SDTM job?
An SDTM job involves working with the Study Data Tabulation Model (SDTM), a standardized format required by regulatory agencies like the FDA for clinical trial data submission. Professionals in this role convert raw clinical data into SDTM-compliant datasets, ensuring consistency, traceability, and adherence to regulatory guidelines. Responsibilities often include data mapping, validation, and quality control to facilitate efficient review by regulatory bodies.
What are the key skills and qualifications needed to thrive in the Sdtm position, and why are they important?
To thrive as an SDTM (Study Data Tabulation Model) Programmer, you need a strong background in clinical data standards, SAS programming, and an understanding of FDA submission requirements, usually supported by a degree in a scientific, mathematical, or computer-related field. Expertise with CDISC standards, SDTM IGs (Implementation Guides), and tools such as Pinnacle 21 Validator or JReview is essential. Strong analytical skills, attention to detail, effective communication, and the ability to collaborate across multidisciplinary teams are vital soft skills. These competencies are crucial for ensuring high-quality, regulatory-compliant clinical trial data that supports successful drug approval processes.
What are the typical daily responsibilities of an SDTM Programmer in a clinical research organization?
As an SDTM Programmer, your daily tasks often include mapping raw clinical data into SDTM domains, validating datasets for compliance with CDISC standards, and generating documentation and specifications for regulatory submissions. You’ll frequently work with clinical data managers, statisticians, and other programmers to ensure data integrity and resolve any data-related queries that arise. Collaboration and timely troubleshooting are key, as your work supports the efficient progression of clinical studies through regulatory review. The role tends to be dynamic and deadline-driven, making organizational skills and adaptability important for success.

Full-time
Posted 16 days ago
Job description
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Candidate must have experience in submissions, statistical programming, EDC, SAS and CRF forms.
The Client Neuroscience Group Business is currently looking to fill an Associate Director, of Data Operations opening at its North American Headquarters in Woodcliff Lake, NJ.
The individual should have expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML.
Excellent technical skills in EDC and SAS systems and application development.
Experience in consulting on projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle at global level for both CRF standards and SDTM standards.
Experience in Review and Quality assurance of datasets and programming specifications produced by other programmers.
Experience in Accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analyses and submissions. Responsible for implementing new technologies for end users and streaming the process from data collection to submission.
Scope and Responsibilities:
- A highly specialized individual contributor or functional manager with advanced knowledge and expertise in a professional discipline.
- Leads execution of key business objectives or projects within the department.
- Involved in developing, modifying, and executing company policies that affect immediate operations and may also have company-wide effect.
The individual must have the following skills:
Expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML.
Excellent technical skills in SAS system and application development.
Proven experience in development and implementation of clinical standards in a global pharmaceutical environment.
Expert in integrating SAS with other leading technologies such as PDF, XML, Microsoft Office, to support electronic submissions.
Experience in consulting on projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle.
Experience in Annotating CRFs in accordance with CDISC published or company specific guidelines with appropriate metadata to reflect case report tabulation data sets.
Experience in Reviewing and quality assurance of CRF annotations produced by other programmers
Embracing and contributing to our culture of process improvements with a focus on streamlining our processes adding value to our business needs.
Experience in Reviewing and quality assurance of datasets, programs and programming specifications produced by other programmers.
Accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analysis and submission.
Accountability for execution of process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analysis and submission
Engaging appropriate stakeholders in communication to create SDTM standards and process for transition of clinical data to SDTM
Accountability for SDTM datasets specification, conversion, and delivery to stakeholders, specifically Statistical Programming, but also other users of SDTM datasets, with high quality and on time.
Providing SDTM data production technology to CDO (Clinical Data Operations) related to SDTM data delivery and manages the activities of a team with a common focus.
For more information, Please contact
Mayank Sharma
973-967-3431
mayank(DOT)sharma1@artecinfo(DOT)com
About Artech
Sourced by ZipRecruiter
Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).
Industry
Recruiting and staffing services
Company size
10,000+ Employees
Headquarters location
Morristown, NJ, US
Year founded
1992