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Cdisc Sdtm Adam Jobs in Reston, VA (NOW HIRING)

CDISC SDTM & ADaM * SAP interpretation * Survival analysis, mixed models, covariate adjustment * Multiplicity control & ICH E9(R1) * Clinical trial data analysis * TFL production & QC * Regulatory ...

Demonstrate expertise in data format standards (e.g., CDISC SDTM ADaM and LAB) and integration with various EDC platforms. * Perform quality control checks to ensure accurate, complete, and compliant ...

Biostatistician

Alexandria, 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 ...

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 ...

Biostatistician

Washington, DC · 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 ...

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 ...

Create CDISC-compliant datasets (SDTM and ADaM) * Validate and document programming outputs * Collaborate with statisticians and data management teams * Support regulatory submissions and audits ...

Develop SAS programs for tables, listings, and figures (TLFs) Create CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data ...

Requirements Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs ...

Cdisc Sdtm Adam information

See Reston, VA salary details

$17

$56

$93

How much do cdisc sdtm adam jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for cdisc sdtm adam in Reston, VA is $56.37, according to ZipRecruiter salary data. Most workers in this role earn between $35.77 and $84.76 per hour, depending on experience, location, and employer.

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 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 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.

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.

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Cities near Reston, VA with the most Cdisc Sdtm Adam job openings:

Clinical Trial Biostatistician with Security Clearance

Cherokee Federal

Bethesda, MD • On-site

Other

Medical, Dental, Vision, Retirement

This job post has expired today. Applications are no longer accepted.


Job description

The Biostatistician will provide statistical and statistical-programming support for a Phase 2a randomized, double-blind clinical trial evaluating a hantavirus vaccine for the prevention of Hemorrhagic Fever with Renal Syndrome (WRAIR 2725). The Biostatistician will develop FDA-ready, CDISC-compliant deliverables, execute analyses per the approved Statistical Analysis Plan (SAP), and support generation of regulatory-submission outputs required for FDA filing and study close-out. This is a fractional, deliverable-driven role with workload concentrated around dataset development, validation, and analysis milestones. Work supports Force Health Protection research and directly enables WRAIR's regulatory submission. Compensation & Benefits: Estimated Starting Salary Range: TBD Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. Benefits are subject to change with or without notice. Clinical Biostatistician Responsibilities Include: Statistical Programming & Validation * 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 datasets to support planned analyses.
* Maintain end-to-end traceability between raw data, SDTM, ADaM, and TLF outputs.
* Perform independent QC and validation checks to ensure accuracy, completeness, and reproducibility. Metadata & Submission Documentation * Create and maintain Define.XML for SDTM and ADaM deliverables.
* Prepare the Study Data Reviewer's Guide (SDRG) for SDTM datasets.
* Prepare the Analysis Data Reviewer's Guide (ADRG) for ADaM datasets.
* Produce annotated CRFs mapping collection fields to SDTM variables and controlled terminology where applicable. Statistical Analysis & Reporting * Review protocol, SAP, SOPs, and study-specific procedures; provide written notification of review and understanding.
* Execute statistical analyses in full alignment with the approved SAP.
* Produce Tables, Listings, and Figures (TLFs) and contribute statistical output and narrative content for the Final Clinical Study Report (FCSR) for regulatory submission. Quality Assurance & Compliance * Ensure all deliverables meet current FDA CDISC standards and related guidance (including define/guide conventions and annotation expectations).
* Produce documentation demonstrating CDISC compliance and audit readiness.
* Meet performance expectations, including a 95% compliance standard against deliverable requirements, on-time submission, and minimal need for substantive revision. Project Coordination & Communication * Coordinate with WRAIR CTC staff on data transfers, review cycles, and issue resolution.
* Provide routine status updates on progress, risks, and dependencies; support inputs to the Program Management Plan (PMP) and Monthly Status Reports (MSRs).
* Communicate effectively with Government leaders, scientists, and stakeholders; clearly identify contractor status in all interactions.
Indicative Deliverable Timeline (from study review start) * SDTM + ADaM datasets, Define.XML, SDRG, ADRG, annotated CRF: within 3 months
* Statistical analyses completed: within 8 months
* FCSR statistical deliverables completed: within 11 months Clinical Biostatistician Experience, Education, Skills, Abilities requested: Required Qualifications * Master's degree in Biostatistics, Statistics, or closely related quantitative field (or equivalent combination of education and experience).
* Demonstrated experience producing CDISC-compliant SDTM and ADaM datasets and associated metadata/documents.
* Strong statistical programming skills for clinical trials; SAS strongly preferred.
* Working knowledge of FDA submission expectations for study data standards and documentation (Define.XML, SDRG/ADRG, CRF annotation).
* Knowledge of GCP, ICH guidelines, and applicable 21 CFR requirements (including Parts 11, 50, 56, and 312).
* Proficiency with Microsoft Office (Outlook, Word, PowerPoint, Excel) and Adobe PDF tools.
* Strong written and verbal communication skills; able to operate effectively with Government stakeholders and cross-functional study teams.
* Ability to work independently, manage shifting priorities, and deliver high-quality work on schedule in a deadline-driven environment. Preferred Qualifications * PhD in Biostatistics or Statistics.
* Experience supporting vaccine, infectious disease, and/or Phase 2 clinical trials.
* Prior experience preparing statistical content for FDA regulatory submissions and clinical study reports.
* Familiarity with DoD/military medical research environments and terminology. Minimum Security Level: * Favorable Tier 1 NACI (or equivalent/higher) completed prior to start, or an open/pending investigation with no unfavorable information, as allowed by the customer.
* Ability to obtain and maintain a Common Access Card (CAC) for on-site facility and network access.
* Must be able to complete a National Agency Check and obtain installation access at WRAIR.
* Mut pass pre-employment requirements of Cherokee Federal. Company Information: Cherokee Nation Integrated Health (CNIH) is a part of Cherokee Federal - the division of tribally owned federal contracting companies owned by Cherokee Nation Businesses. As a trusted partner for more than 60 federal clients, Cherokee Federal LLCs are focused on building a brighter future, solving complex challenges, and serving the government's mission with compassion and heart. To learn more about CNIH, visit cherokee-federal.com. #CherokeeFederal #LI-IG1 Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. Legal Disclaimer: Cherokee Federal is an equal opportunity employer. Please visit cherokee-federal.com/careers for information regarding our Affirmative Action and Equal Opportunity Employer Statement, and Accommodation request. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Please Note: This position is pending a contract award. If you are interested in a future with Cherokee Federal, APPLY TODAY! Although this is not an approved position, we are accepting applications for this future and anticipated need.

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About Cherokee Federal

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Cherokee Federal - a division of Cherokee Nation Businesses - is a team of tribally owned federal contracting companies focused on building solutions, solving complex challenges, and serving the nation's mission around the globe for more than 60 federal clients. Our team of companies manages nearly 1,000 projects of all sizes across the construction, consulting, engineering and manufacturing, health, and technology portfolios. Since 2012, the Cherokee Federal team of companies has won more than $5 billion in government contracts. Our 3,000+ employees work in 26 countries, 50 states and 2 U.S. territories. Why choose Cherokee Federal? Visit our website and learn about the great reasons to join our team. cherokee-federal.com

Industry

Architectural services

Company size

1,001 - 5,000 Employees

Headquarters location

Tulsa, OK, US

Year founded

1969

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