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Sdtm Jobs in Texas (NOW HIRING)

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets * Ensure compliance with GCP, regulatory requirements, and company SOPs * Support inspection readiness and ...

Clinical Data Manager

Austin, TX · On-site

$125K - $175K/yr

Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets * Ensure compliance with GCP, regulatory requirements, and company SOPs * Support inspection readiness and ...

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets * Ensure compliance with GCP, regulatory requirements, and company SOPs * Support inspection readiness and ...

SME on operational data standards utilizing SDTM standards and CDISC controlled terminology in developing operational data standards. * Contributing to developing and applying smart systems and ...

Contribute to the creation, validation, and documentation of SDTM and ADaM datasets. * Responsible for producing programming outputs, validation, and related documentation to ensure accuracy ...

Contribute to the creation, validation, and documentation of SDTM and ADaM datasets. * Responsible for producing programming outputs, validation, and related documentation to ensure accuracy ...

Contribute to the creation, validation, and documentation of SDTM and ADaM datasets. * Responsible for producing programming outputs, validation, and related documentation to ensure accuracy ...

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 ...

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 ...

Biostatistician

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 ...

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

Waco, 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 ...

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

Edinburg, 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 ...

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

Denton, 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 ...

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

Pearland, 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 ...

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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Sdtm information

See Texas salary details

$17

$50

$74

How much do sdtm jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for sdtm in Texas is $50.34, according to ZipRecruiter salary data. Most workers in this role earn between $38.75 and $63.37 per hour, depending on experience, location, and employer.

What is an SDTM?

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 as an SDTM programmer?

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 does an SDTM programmer do?

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.

Infographic showing various Sdtm job openings in Texas as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $104,717 per year, or $50.3 per hour.

Clinical Data Manager

Faeth Therapeutics

Austin, TX • Remote

$125K - $175K/yr

Full-time

Medical, Dental, Vision, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M in funding. With a strong scientific foundation and a founding team that includes the discoverer of our target pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, toward multiple near-term milestones. We are a small, focused team where every person has direct impact — united by a shared commitment to care deeply, create boldly, and never stop learning.

Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ensuring high-quality, reliable clinical data through the design, implementation, and oversight of data management processes. The role requires close collaboration with clinical operations, biostatistics, medical, and external vendors.

Reports to: Chief Medical Officer

Location: Remote (U.S.)

Responsibilities:

  • Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b)
  • Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance
  • Review and contribute to key study documents, including:
  • Data Management Plans (DMPs)
  • Case Report Forms (CRFs) / eCRFs
  • Edit check specifications
  • Data transfer specifications
  • Manage database build, UAT, and database lock activities
  • Ensure data integrity, consistency, and completeness through ongoing data review and cleaning
  • Monitor query generation and resolution timelines
  • Perform data review, listings review, and support medical data review activities
  • Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets
  • Ensure compliance with GCP, regulatory requirements, and company SOPs
  • Support inspection readiness and participate in audits/inspections as needed
  • Contribute to process improvements and best practices in data management

Requirements:

  • Bachelor’s degree in life sciences, computer science, or related field (advanced degree a plus)
  • 5–8 years of clinical data management experience in biotech, pharma, or CRO settings
  • Experience supporting early- to mid-phase clinical trials (Phase 1–2 required)
  • Hands-on experience with EDC systems (e.g., Medidata Rave, Veeva, Oracle InForm)
  • Strong understanding of clinical data standards (CDISC, SDTM)
  • Experience managing CROs and external vendors
  • Familiarity with oncology trials is preferred
  • Knowledge of GCP and regulatory requirements
  • Strong attention to detail and problem-solving skills
  • Excellent communication and cross-functional collaboration skills

Compensation Range: $125,000 - $175,000 (actual compensation may vary based on experience, qualifications and location)

Working at Faeth

Benefits:

  • Competitive salary and equity in a well-funded, clinical-stage biotech
  • 100% remote work and flexible schedule
  • Health, dental, and vision for you and your dependents
  • Flexible time off
  • Generous parental leave
  • Traditional and Roth 401k 
  • Mission oriented, remote first culture

We are an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

All offers of employment are contingent upon satisfactory completion of a background check and verification of eligibility to work in the United States.