ZipRecruiter

Log In

2

Remote Sdtm Jobs (NOW HIRING)

VENESCO, LLC

SAS Programmer

Falls Church, VA · On-site +1

Remote/Hybrid Job Type: Full-Time Position Overview: Venesco is seeking a skilled SAS Programmer to ... Develop SAS programs for tables, listings, and figures (TLFs) Create CDISC-compliant datasets (SDTM ...

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

... SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values * We believe in applying scientific rigor to reveal the full promise ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ... Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets * Ensure ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ... Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets * Ensure ...

Goldbelt, Inc.

Biostatistician

Silver Spring, MD · On-site +1

$50/hr

SDTM datasets * ADaM datasets * Define.xml documentation * SDRG/ADRG documentation * Generate and ... Remote work may be permitted, subject to task requirements and Government approval. Position Type:

MM International

Data Scientist

New York, NY · Remote

Remote Duration 4-6 months The RBQM Data Scientist supports central monitoring and risk-based ... CDISC, CDASH, SDTM standards. • Exposure to R, Python, or JavaScript and/or clinical data ...

next page

Showing results 1-20

All JobsSdtm JobsRemote Sdtm Jobs

Remote Sdtm information

See salary details

$19

$54

$80

How much do remote sdtm jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for remote sdtm in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What is the difference between Remote Sdtm vs Remote Clinical Data Coordinator?

AspectRemote SdtmRemote Clinical Data Coordinator
CertificationsCDISC SDTM, CDMPCDISC SDTM, CDMP
Work EnvironmentRemote, data management teamsRemote, clinical data management teams
Industry UsagePharmaceutical, biotechPharmaceutical, biotech
Primary ResponsibilitiesDesign, validate SDTM datasetsManage, clean, and verify clinical data

Remote Sdtm specialists focus on creating and validating SDTM datasets for clinical trials, while Remote Clinical Data Coordinators handle overall data management, including data entry, cleaning, and verification. Both roles require similar certifications and work in the same industry, but their core tasks differ in scope and focus.

How does a Remote SDTM professional typically collaborate with cross-functional teams to ensure accurate clinical data submission?

As a Remote SDTM (Study Data Tabulation Model) professional, you will regularly work with clinical data managers, biostatisticians, and programmers to ensure that clinical trial data is accurately mapped and compliant with regulatory standards. Collaboration often involves virtual meetings, shared documentation, and version control tools to review data mappings and resolve discrepancies. Clear communication and proactive problem-solving are vital, as much of the alignment happens remotely. You'll also participate in data validation and quality control processes to support successful data submissions to regulatory authorities.

What are the key skills and qualifications needed to thrive as a Remote SDTM (Study Data Tabulation Model) Specialist, and why are they important?

To thrive as a Remote SDTM Specialist, you need strong expertise in clinical data management, SDTM standards, and familiarity with regulatory requirements, often supported by a degree in life sciences or a related field. Proficiency in tools like SAS, clinical data management systems (CDMS), and CDISC-compliant software is typically required. Excellent attention to detail, problem-solving abilities, and effective remote communication skills help individuals excel in this role. These competencies ensure accurate data standardization, regulatory compliance, and seamless collaboration within distributed teams.

What is a Remote SDTM professional?

A Remote SDTM (Study Data Tabulation Model) professional is a specialist who works remotely to standardize and organize clinical trial data according to the SDTM guidelines set by the Clinical Data Interchange Standards Consortium (CDISC). This role is crucial in preparing datasets for regulatory submissions by ensuring that data collected in clinical studies is consistently formatted and easily understood. Remote SDTM professionals are responsible for mapping raw clinical data into SDTM domains, performing quality checks, and collaborating with data managers and statisticians. Working remotely allows them to support clinical trials for pharmaceutical or biotechnology companies from anywhere, using secure digital tools.
More about Remote Sdtm jobs
What cities are hiring for Remote Sdtm jobs? Cities with the most Remote Sdtm job openings:
What are the most commonly searched types of Sdtm jobs? The most popular types of Sdtm jobs are:
What states have the most Remote Sdtm jobs? States with the most job openings for Remote Sdtm jobs include:
What job categories do people searching Remote Sdtm jobs look for? The top searched job categories for Remote Sdtm jobs are:
Remote Sdtm jobs near you
Infographic showing various Remote Sdtm job openings in the United States as of July 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 51% Physical, 4% Hybrid, and 45% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.
Senior Clinical Programmer - SDTM and R/SAS 3635027

Senior Clinical Programmer - SDTM and R/SAS 3635027

Axiom Path

Bridgewater, NJ • Remote

$75 - $80/hr

Full-time

Posted 12 days ago

Job description

Be Part Of A High-Performing Team:

Join a growing clinical programming function within a science-driven biopharmaceutical organization developing therapies for patients with serious and rare diseases. This newly established team is bringing critical SDTM programming capabilities in-house and works closely with data management, biostatistics, and statistical programming. The environment is collaborative, technically rigorous, and well suited to an experienced programmer who enjoys building reliable clinical-data solutions while helping shape new internal processes.

What's In Store For You:

Engagement: W2 only (no C2C/1099)

This is a fully remote, 12-month consulting assignment open to candidates located anywhere in the United States. Availability during Eastern Time business hours is preferred.

The role offers the opportunity to become one of the early members of a growing clinical programming team and contribute directly to the organization’s transition from outsourced SDTM programming to an internal delivery model. A contract extension may be possible based on performance and business needs, although permanent conversion is not currently planned.

How You Will Make An Impact:

  • Create production-quality SDTM datasets using both SAS and R.
  • Independently perform quality control and validation of SDTM datasets.
  • Develop dataset specifications using CDISC standards and current SDTM Implementation Guides.
  • Create annotated CRFs, including domain mappings, annotation boxes, controlled terminology, and page-level placement.
  • Apply existing team macros and programming utilities to support annotated CRF and SDTM production.
  • Develop SAS- and R-based listings and reports supporting medical monitoring, clinical data management, and statistical endpoint monitoring.
  • Perform clinical-data checks, reconciliations, and issue investigation as assigned.
  • Collaborate closely with data managers, biostatisticians, statistical programmers, and clinical-study stakeholders.
  • Help establish scalable internal standards, workflows, and quality practices as SDTM programming transitions in-house.
  • Manage multiple study deliverables independently while maintaining accuracy, traceability, and timely execution.

Do you bring proven success in SDTM programming with both SAS and R?

  • Approximately 8–10 years of hands-on clinical programming experience in pharmaceutical, biotechnology, CRO, or related regulated clinical environments.
  • Strong production programming proficiency in both SAS and R.
  • Demonstrated experience creating and independently quality-checking SDTM datasets.
  • Strong knowledge of CDISC standards and current SDTM Implementation Guides.
  • Hands-on experience creating annotated CRFs, including page-level annotations and terminology mapping.
  • Ability to use established macros, functions, and programming utilities.
  • Experience translating raw clinical data, CRFs, specifications, and programming standards into compliant SDTM deliverables.
  • Strong analytical, troubleshooting, documentation, and quality-control skills.
  • Ability to work independently as an individual contributor in a small and evolving team.
  • Strong written and verbal communication skills.
  • Experience with JReview is highly preferred.
  • Experience with Shiny, Pharmaverse, or R Markdown is highly desirable.
  • Exposure to SQL programming is preferred.
  • Experience supporting medical monitoring, data-management reports, reconciliations, or statistical endpoint monitoring is beneficial.

#dice