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Remote Sdtm Jobs in Raleigh, NC (NOW HIRING)

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and ... Application Deadline:8/15/26#LI Remote Learn more about our EEO & Accommodations request here.

Biostatistician

Durham, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... SDTM/ADaM datasets. * Solid understanding of statistical methods used in confirmatory trials ...

Biostatistician

Raleigh, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... SDTM/ADaM datasets. * Solid understanding of statistical methods used in confirmatory trials ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... SDTM/ADaM datasets. * Solid understanding of statistical methods used in confirmatory trials ...

Director of Biostatistics

Cary, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... SDTM/ADaM datasets. * Solid understanding of statistical methods used in confirmatory trials ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... SDTM/ADaM datasets. * Solid understanding of statistical methods used in confirmatory trials ...

Biostatistician

Cary, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... SDTM/ADaM datasets. * Solid understanding of statistical methods used in confirmatory trials ...

Remote Sdtm information

See Raleigh, NC salary details

$18

$52

$78

How much do remote sdtm jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote sdtm in Raleigh, NC is $52.53, according to ZipRecruiter salary data. Most workers in this role earn between $40.43 and $66.11 per hour, depending on experience, location, and employer.

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.

How does a Remote SDTM professional 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 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 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.

What are popular job titles related to Remote Sdtm jobs in Raleigh, NC?

For Remote Sdtm jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Sdtm jobs in Raleigh, NC look for?

The top searched job categories for Remote Sdtm jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Sdtm jobs?

Cities near Raleigh, NC with the most Remote Sdtm job openings:

Infographic showing various Remote Sdtm job openings in Raleigh, NC as of August 2026, with employment types broken down into 87% Full Time, 6% Part Time, and 7% Contract. Highlights an 100% Remote job distribution, with an average salary of $109,261 per year, or $52.5 per hour.

Senior Programmer Analyst

Fortrea

Durham, NC • Remote

$80K - $95K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 74 rated research


Job description

Job Overview:

Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and reconciliations. Perform any postproduction changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, SAS Datasets etc., Conduct Peer Review/Quality control of study design for assigned projects.

    Summary of Responsibilities:

    • Lead the development and implementation of Clinical solutions to global technical services issues and concerns regarding EDC tools or SAS programming.
    • Lead the development of visual analytics dashboard using tools like Spotfire/Tableau.
    • Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software according to Fortrea SOPs, Work Instructions, and project specific guidelines in accordance with Good Clinical Practices.
    • Perform any post-production changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, etc.,
    • With assistance, meet with Data Manager on assigned projects to discuss contractual obligations and timelines.
    • Act as Subject Matter Expert (SME) and be point of contact for any technical services, issues related to EDC tools or SAS programming.
    • Serve as Lead Statistical Programmer providing programming support for development and maintenance of SDTM/Client standards datasets.
    • Develop/validate Custom/Complex SDTM domains and efficiently handle external data and data reconciliations.
    • Develop and implement SDTM automation/standardization and best programming practices across projects to enhance quality and productivity.
    • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
    • Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills.
    • Participate in the ongoing review of the processes used to ensure adaptation of best practices.
    • Conduct Peer Review/Quality control of study design for assigned projects.
    • Able to work independently and take initiative to accept new challenges in Clinical Programming Applications, also participate in the validation of new or updates to software.
    • Maintain awareness of new developments in EDC products which may be applied to improve the efficient use of these systems.
    • Resource forecasting and allocate activities to the team members on the project.
    • Proactively identify trends, generate reports/metrics, or demonstrate programming processes to sponsors/auditors (if required), assist with the design of ECRFs and other study documents.
    • And all other duties as needed or assigned

    Qualifications (Minimum Required):

    • University / college degree (life sciences, health sciences, information technology or related subjects preferred).
    • Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor's degree.
    • Fluent in English, both written and verbal.
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

    Experience (Minimum Required):

    • 5 to 8 years of relevant work experience to include data management and database support or SAS Programming or Spotfire or Tableau development.
    • Good problem-solving skills and a proactive approach.
    • Good oral and written communication skills.
    • Basic knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred.
    • Demonstrated ability to work in a team environment.
    • Demonstrated ability to work independently under supervision.
    • Proven interpersonal skills.

    Physical Demands/Work Environment:

    • Office work environment.
    Pay Range:$80,000-$95,000Benefits:All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular,full-timeor part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.Application Deadline:8/15/26#LI Remote

    Learn more about our EEO & Accommodations request here.


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