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Cdisc Sdtm Adam Jobs (NOW HIRING)

SystImmune, Inc

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

Working knowledge of CDISC standards (SDTM and ADaM). * Hands-on experience in developing and validating SDTM and ADaM datasets, as well as statistical outputs (tables, figures, and listings)

micro1 AI

Director of Biostatistics

Chattanooga, TN · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Thornton, CO · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Boise, ID · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Lubbock, TX · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Irving, TX · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Spokane Valley, WA · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Raleigh, NC · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Gilbert, AZ · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Joliet, IL · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

El Paso, TX · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Director of Biostatistics

Roanoke, VA · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

micro1 AI

Biostatistician

Winston Salem, NC · Remote

$60 - $65/hr

Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets. * Solid understanding of statistical methods used in ...

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How much do cdisc sdtm adam jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for cdisc sdtm adam in the United States is $54.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $81.49 per hour, depending on experience, location, and employer.

What are the typical collaboration points between a CDISC SDTM/ADaM programmer and clinical data managers during a clinical trial project?

A CDISC SDTM/ADaM programmer works closely with clinical data managers to ensure data collected during a clinical trial is accurately mapped and transformed according to regulatory standards. Collaboration often involves clarifying data definitions, resolving data discrepancies, and aligning on timelines for data delivery. Regular meetings and clear communication are key, as programmers rely on data managers for clean, validated data, while data managers depend on programmers to structure data sets correctly for analysis and regulatory submission. This partnership is essential for meeting project deadlines and maintaining data integrity.

What are CDISC SDTM and ADaM?

CDISC SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) are data standards used in clinical trials to organize and submit data to regulatory agencies like the FDA. SDTM defines how to structure raw clinical trial data for submission, focusing on standardizing data tabulation. ADaM provides guidelines for creating datasets used in statistical analysis, ensuring the data is analysis-ready and traceable back to SDTM. Both standards improve data quality, consistency, and regulatory review efficiency in the pharmaceutical industry.

What is the difference between Cdisc Sdtm Adam vs Clinical Data Coordinator?

AspectCdisc Sdtm AdamClinical Data Coordinator
Primary RoleDevelops and manages ADaM datasets for clinical trialsOversees data collection, entry, and quality control in clinical studies
Required SkillsKnowledge of CDISC standards, SAS programming, statistical conceptsData management, database systems, attention to detail
Work EnvironmentPharmaceutical or CRO data analysis teamsClinical research sites, CROs, pharmaceutical companies

While Cdisc Sdtm Adam specialists focus on creating analysis datasets using CDISC standards, Clinical Data Coordinators manage the overall data collection and quality in clinical trials. Both roles require knowledge of clinical data processes but differ in their specific responsibilities and technical focus.

What are the key skills and qualifications needed to thrive as a CDISC SDTM/ADaM specialist, and why are they important?

To thrive as a CDISC SDTM/ADaM Specialist, you need a solid background in clinical data management, knowledge of regulatory standards, and expertise in statistical programming (often with SAS). Familiarity with CDISC SDTM and ADaM models, FDA submission requirements, and tools like Pinnacle 21 or JReview is typically required. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for this role. These competencies ensure accurate data standardization, regulatory compliance, and smooth collaboration in clinical research environments.
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Cdisc Sdtm Adam jobs near you
Infographic showing various Cdisc Sdtm Adam job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 10% Part Time, and 3% Contract. Highlights an 75% Physical, 1% Hybrid, and 24% Remote job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

Senior SAS/Statistical Programmer

Wizsolution

Plainsboro, NJ • Remote

Full-time

Re-posted 28 days ago

Job description

Job Description

Company Descriptions:

Wizsolution is located in Princeton NJ, which is a leader in pharmaceutical recruitment and staffing. Our goal is to provide effective solutions for fulfilling your career potential. The mission of our company is to connect high talent and motivated candidates to technical positions from our partner companies.

Job descriptions:

Senior SAS Programmer
Senior Statistical Programmer

*

-Perform SAS data manipulation and analysis programming
-May work with medical writing, clinical operations, and other clinical staff to support deliverables.
-Must work well both independently and with team members.
-Needs to be able to be on-time with deliverables, and for those deliverables to be of quality.
-Works with Statistician and Statistical programmer to assure results are consistent with expectations, and Quality control procedures are followed.
-Plans and carefully documents differences between programming results between program developer and Statistical QC programmer.
-Confirms that tracking sheets are current for projects, and may also confirm that results are consistent with earlier generated results.

·             MS with 3-5 +years of pharmaceutical industry experience.

·             Strong collaboration abilities and ability to work as part of a highly skilled team.

·             Experience in CDISC (SDTM, ADaM data sets)

·             Skilled in analysis of safety, efficacy & biomarker data, with an understanding of multiplicity issues; immunology/CV background a plus.

·             Experienced with standard and advanced statistical methods.

·             Expertise in SAS required, S-Plus or R preferred, including advanced statistical analysis, data integration, graphing & simulation.

·             Strong programming skills.

·             Good understanding of regulatory requirements & clinical trial design.

·             Knowledge of and ability to learn relevant clinical background and biomarker biology and incorporate these into statistical design, analysis & interpretation.

Preferred Qualifications:

Must have 3-5+ years SAS Programmer experience
SAS systems experience may include Base SAS, SAS/FSP,SAS SCL, Macro Facility, SAS/Graph, SAS / ODS, and SAS / Stat within a Windows operating system.

Job Type: Full-time