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Cdisc Jobs in Texas (NOW HIRING)

Data Architect

Austin, TX · On-site

$100 - $130/hr

Apply CDISC standards (SDTM, ADaM concepts, Define-XML awareness) and evaluate OMOP/FHIR applicability for interoperability initiatives * Partner with integration engineers on API contracts, event ...

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

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

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

Statistical Programmer II

Austin, TX · On-site

$90K - $100K/yr

Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...

... CDISC standards o HIPAA o ICH-GCP o GDPR (where applicable) o Internal SOPs and quality requirements, including documentation of data accuracy, integrity, security, audit trails, and regulatory ...

Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...

Working knowledge of CDISC standards, especially SDTM and ADaM. * Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses. * Understanding of clinical trial ...

Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas. * Understand the various tools that we work with * High level ...

Cdisc information

See Texas salary details

$78.7K

$137.2K

$232K

How much do cdisc jobs pay per year?

As of Aug 31, 2026, the average yearly pay for cdisc in Texas is $137,225.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,500.00 and $149,100.00 per year, depending on experience, location, and employer.

What is a CDISC?

A CDISC job typically involves working with clinical data following CDISC (Clinical Data Interchange Standards Consortium) standards, which ensure consistency and compliance in regulatory submissions. Professionals in CDISC roles manage datasets in formats like SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) to facilitate data analysis and reporting. These roles are common in pharmaceutical, biotech, and clinical research organizations, often requiring expertise in programming languages like SAS and knowledge of FDA submission guidelines.

What are the key skills and qualifications needed to thrive in the CDISC position, and why are they important?

To thrive as a CDISC specialist, you need expertise in clinical data standards, data management, and a strong background in life sciences or clinical research. Familiarity with CDISC standards like SDTM, ADaM, and tools such as SAS, Medidata, or clinical data management systems is essential, and certifications in CDISC or related areas are highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills for collaborating with cross-functional teams. These competencies ensure accurate data standardization and compliance in clinical trials, facilitating regulatory submissions and high-quality research outcomes.

What are some common challenges faced by CDISC specialists in clinical research?

CDISC specialists often face challenges such as keeping up with evolving data standards, ensuring data consistency across multiple studies, and coordinating with global teams to align on standard implementation. It is common to manage large, complex datasets while working under tight deadlines to meet regulatory submission timelines. Successfully overcoming these challenges requires strong technical acumen, effective communication with clinical and statistical teams, and proactive problem-solving. If you enjoy collaborating in a dynamic environment and have a passion for data quality and compliance, this role can offer significant professional growth opportunities.

What are the most commonly searched types of Cdisc jobs in Texas?

The most popular types of Cdisc jobs in Texas are:

Infographic showing various Cdisc job openings in Texas as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $137,225 per year, or $66 per hour.

Data Architect

Nexa Trials

Austin, TX • On-site

$100 - $130/hr

Other

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


Job description

Own the clinical data layer that connects NexaSource capture, Nexa Bus integrations, and sponsor EDC systems — translating protocols and CRFs into durable, standards-aligned schemas that scale across studies.

United States Austin, TX

About the role

Nexa Trials is seeking an experienced Data Architect to design and govern the clinical data models that power our platform and services. You will sit at the intersection of eSource, EDC, and sponsor reporting — defining how data captured in NexaSource™ maps through Nexa Bus™ into Medidata Rave, Veeva, Oracle Clinical One, and custom sponsor environments.

Your work directly reduces duplicate entry, query volume, and study startup friction. You will partner with clinical operations, QC analysts, integration engineers, and AI/automation teams in Lahore to ensure every mapping decision is traceable, GCP-aligned, and maintainable across protocol amendments and multi-site rollouts.

This role is based in Austin, Texas — Nexa Trials headquarters — with flexibility for hybrid or remote work within US time zones. You will report to the Head of Data & Integrations and contribute to our standards roadmap across CDISC, OMOP, and FHIR.

Responsibilities
  • Design end-to-end data models for eSource forms, visit schedules, and Nexa Bus transfer pipelines from protocol and CRF specifications
  • Author and maintain EDC/eSource field mappings, transformation rules, and validation logic for sponsor and CRO study builds
  • Define canonical data structures that support NexaSource capture, NexaScheduler visit events, and downstream analytics
  • Apply CDISC standards (SDTM, ADaM concepts, Define-XML awareness) and evaluate OMOP/FHIR applicability for interoperability initiatives
  • Partner with integration engineers on API contracts, event schemas, and error-handling patterns for live study transfers
  • Review QC findings and query trends to identify systemic mapping gaps and recommend architectural improvements
  • Document data lineage, mapping decisions, and amendment impact assessments for audit-ready sponsor deliverables
  • Contribute to reusable mapping libraries, study templates, and governance processes that accelerate study startup
  • Mentor junior data analysts and collaborate with Clinical AI engineers on structured outputs for LLM-assisted mapping tools
Requirements
  • 5+ years of experience in clinical data architecture, EDC build, or clinical data management on Phase I–IV trials
  • Deep working knowledge of CDISC standards and practical experience translating CRFs into structured clinical datasets
  • Hands‑on experience with EDC/eSource mapping — field‑level transformations, edit checks, and cross‑form dependencies
  • Proficiency with at least two major EDC platforms (e.g., Medidata Rave, Veeva Vault CDMS, Oracle Clinical One, REDCap)
  • Strong SQL skills and familiarity with data integration patterns (REST APIs, flat‑file exchange, ETL pipelines)
  • Ability to read protocols and SAPs and translate clinical intent into implementable data specifications
  • Excellent documentation habits — mapping specs, data dictionaries, and change logs that satisfy sponsor audit expectations
  • Eligible to work in the United States
Nice to have
  • Experience with OMOP CDM, FHIR resources, or real‑world data interoperability projects
  • Exposure to NexaSource, custom eSource platforms, or site‑centric capture workflows
  • Knowledge of ICH E6(R2) GCP requirements for data integrity and ALCOA+ principles
  • Python or similar scripting for mapping validation, diff analysis, or automated spec generation
  • Prior work with CROs, mid‑size sponsors, or multi‑site network rollouts
  • Familiarity with AI‑assisted mapping or clinical NLP for document extraction
What we offer

Join a clinical technology company where data architecture decisions ship to production on live studies — not sit in enterprise backlog limbo. You will shape the foundation that Nexa Bus, NexaSource, and our QC operations depend on.

  • Competitive salary, equity consideration, and comprehensive US health benefits
  • Hybrid or remote flexibility anchored to our Austin headquarters
  • Direct influence on product data models and integration strategy
  • Collaboration with engineering teams in Lahore and QC operations in Dubai
  • Conference and certification support for CDISC, FHIR, and clinical data management credentials
  • Clear path to lead architect or Head of Data & Integrations as the portfolio grows
Location

Austin, Texas, United States Region: North America Country: United States City: Austin, TX Hybrid / remote within US time zones — periodic presence at Austin HQ

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