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Senior Sdtm Programmer Jobs (NOW HIRING)

Genentech, Inc.

Senior ADS Programmer

Boston, MA · On-site

... SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs ... You develop and support programming outputs across a wide range of data types, including ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA

$145K - $156K/yr

Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and ... Establish and enforce data standardization practices (e.g., CDISC, SDTM, ADaM) * Collaborate with ...

Lancesoft

Senior Statistical Programmer

Irvine, CA · On-site

$75 - $98.48/hr

Senior Statistical Programmer Dura tion: Jun 8 Dec 31, 2026 Location: Irvine, CA, 92618 Schedule ... G., SDTM, ADaM). * Experience supporting programming deliverables that are inspection ready.

Genentech

Senior ADS Programmer

Boston, MA

... SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs ... You develop and support programming outputs across a wide range of data types, including ...

EDETEK

Senior Statistical Programmer

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team. As a ... Develop and validate SAS programs to generate SDTM, ADaM datasets, tables, listings, and figures ...

Servier

Sr. Manager, Statistical Programming

Boston, MA · On-site

$151K - $172K/yr

Role Summary The Sr Manager, Statistical Programming is responsible for the development of ... Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM and ADaM ...

Legend Biotech USA, Inc.

Role OverviewThe Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in ... SDTM, ADaM)Experience with or strong willingness to leverage AI-assisted programming tools to ...

CICONIX, LLC

Senior Biostatistician About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... programming specifications used to create CDISC-compliant datasets, SDTM, Analysis Data Model ...

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Senior Sdtm Programmer information

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How much do senior sdtm programmer jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for senior sdtm programmer in the United States is $52.28, according to ZipRecruiter salary data. Most workers in this role earn between $43.99 and $62.50 per hour, depending on experience, location, and employer.

What is the difference between Senior Sdtm Programmer vs Clinical Data Coordinator?

AspectSenior Sdtm ProgrammerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in SDTM programmingUsually holds a degree in health sciences, nursing, or related field, with data management training
Work EnvironmentWorks primarily in clinical trial data programming, using SAS or similar toolsManages data entry, cleaning, and validation in clinical trial settings
Industry UsageCommonly employed in pharmaceutical and biotech companies for SDTM data standardizationFound in clinical research organizations, hospitals, and pharmaceutical companies

The main difference is that Senior Sdtm Programmers focus on programming and data standardization using SDTM standards, while Clinical Data Coordinators handle data collection, entry, and quality control. Both roles are essential in clinical trials but differ in technical scope and responsibilities.

What are the typical collaboration points between a Senior SDTM Programmer and clinical data management teams?

As a Senior SDTM Programmer, you frequently collaborate with clinical data management teams to ensure data collected from clinical trials is accurately mapped and transformed into SDTM-compliant datasets. This often involves clarifying data specifications, resolving data discrepancies, and aligning on timelines for data delivery. Close communication helps maintain data integrity and compliance with regulatory standards, making teamwork and proactive problem-solving crucial aspects of the role.

What are Senior SDTM Programmers?

Senior SDTM Programmers are experienced professionals in clinical data management who specialize in mapping and converting clinical trial data into the Study Data Tabulation Model (SDTM) format according to regulatory requirements. They ensure that data collected during clinical trials is structured, accurate, and compliant with standards set by organizations like the FDA and CDISC. Senior SDTM Programmers often lead programming activities, perform quality control checks, and collaborate with statisticians, data managers, and regulatory teams to prepare submission-ready datasets. Their expertise is vital for successful clinical trial submissions and regulatory approvals.

What are the key skills and qualifications needed to thrive as a Senior SDTM Programmer, and why are they important?

To excel as a Senior SDTM Programmer, you need deep expertise in clinical data standards (especially CDISC SDTM), advanced SAS programming skills, and a relevant degree in life sciences, statistics, or computer science. Familiarity with clinical trial data management systems, regulatory submission requirements, and tools like Pinnacle 21 are also crucial. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data accuracy and smooth collaboration with cross-functional teams. These competencies are essential to deliver high-quality, regulatory-compliant datasets that support successful clinical trial submissions.
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Infographic showing various Senior Sdtm Programmer job openings in the United States as of May 2026, with employment types broken down into 100% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $108,736 per year, or $52.3 per hour.

Senior Principal Programmer

Braveheart Bio

San Francisco, CA • On-site, Remote

$250K - $295K/yr

Full-time

Posted 26 days ago

Job description

About us:
Braveheart Bio is a Bay Area-based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. Our lead program is a next-generation myosin inhibitor, licensed from Hengrui Pharma, being developed to transform the treatment of hypertrophic cardiomyopathy (HCM)-the most common inherited cardiac disease.
Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our candidate has demonstrated a compelling clinical profile that may position it as a best-in-class therapy with meaningful differentiation.
With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a high-profile and rapidly evolving therapeutic area.
The role:
The Senior Principal Programmer will report into the VP, Biometrics and provide strategic and technical leadership for clinical programming activities across clinical development programs. This individual will oversee CRO programming deliverables, support global regulatory submissions, contribute to ongoing study monitoring, and collaborate closely with Biostatistics, Data Management, Clinical Operations, Regulatory, and external vendors to ensure high-quality, compliant, and timely delivery of clinical data outputs.
Key responsibilities:
  • Oversee CRO programming activities, including SDTM, ADaM, TFLs, define.xml, reviewer's guides, and other clinical study or submission deliverables.
  • Review CRO programming plans, specifications, datasets, outputs, QC documentation, issue logs, and submission packages.
  • Ensure programming deliverables are accurate, traceable, reproducible, and compliant with CDISC standards and FDA/EMA expectations.
  • Serve as the internal programming lead for FDA, EMA, and other regulatory submissions, including support for health authority questions and ad hoc analyses.
  • Support ongoing study monitoring by reviewing safety, efficacy, DMC, interim analysis, patient profile, and data review outputs prepared by the CRO.
  • Collaborate with Data Management to support data cleaning, external data review, reconciliation, database lock, and data quality activities.
  • Work closely with Biostatistics, Clinical Operations, Regulatory, Safety, Data Management, CROs, vendors, and external partners to align timelines, deliverables, standards, and responsibilities.
  • Coordinate with alliance or development partners on programming-related deliverables, review comments, issue resolution, and submission-readiness activities.
  • Track CRO performance, identify programming risks, resolve issues, and ensure timely delivery of high-quality outputs.
  • Provide programming input into protocols, SAPs, data standards, TFL shells, DMC charters, submission plans, and regulatory response strategies.

Required experience & skills:
  • At least 10 years of experience in clinical statistical programming in biotechnology/ pharmaceutical industry
  • Strong expertise in SAS, CDISC SDTM/ADaM standards, TFLs, define.xml, SDRG, ADRG, and regulatory submission requirements
  • Experience overseeing CRO programming deliverables and supporting FDA/EMA submissions
  • Strong expertise in clinical trials, data management processes, database lock, interim analyses, DMC support, and regulatory responses
  • Strong written and verbal communication skills with a collaborative, team-oriented approach
  • Ability to thrive in a fast-paced, dynamic environment and remain comfortable with change and ambiguity
  • Flexible, proactive, and comfortable operating with lean internal resources and contributing hands-on as needed

Preferred experience & skills:
  • Prior experience serving as programming lead or submission programming lead
  • Experience overseeing multiple studies or programs in parallel
  • Experience working with global CROs, vendors, and external development partners
  • Ability to read/communicate in Chinese is helpful

Base Salary Range: $250K - $295K
This role is eligible for a competitive total rewards package, including an annual bonus, equity, and a comprehensive benefits offering.
We are an equal opportunity employer.
We are committed to inclusion and diversity, and we do not discriminate on the basis of race, gender, religion, gender, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any characteristic protected under applicable law.
Braveheart participates in the federal E-Verify program to confirm employment authorization for all new hires.
To learn more about E-Verify please review this poster.

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