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Full Time Sdtm Programmer Jobs (NOW HIRING)

Clinical Data Analyst, Spotfire

Redmond, WA ยท On-site

$90K - $130K/yr

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities ... programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM ...

Clinical Data Analyst, Spotfire

Redmond, WA ยท On-site

$90K - $130K/yr

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities ... programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM ...

New Jersey, US | full time | Job ID: 9895 About this Role: As Director Biostatistics (Oncology) you ... Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a ... SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

This position requires you to be onsite full-time in Redmond, WA.Responsibilities: * Leads all DM ... Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a ... SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ...

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Full Time Sdtm Programmer information

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$16

$54

$89

How much do full time sdtm programmer jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for full time sdtm programmer in the United States is $54.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $81.49 per hour, depending on experience, location, and employer.

Are SAS programmers in demand?

SAS programmers, including SDTM programmers who work with clinical trial data, are in steady demand due to the ongoing need for data management and analysis in the pharmaceutical and healthcare industries. Skills in SAS, data standards like SDTM, and familiarity with regulatory requirements increase employability in this field.

How much do SAS programmers make?

SAS programmers, including those working as full-time SDTM programmers, typically earn between $70,000 and $120,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced programmers with specialized skills can earn higher salaries, especially in the pharmaceutical or clinical research industries where SDTM programming is common.

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

AspectFull Time Sdtm ProgrammerClinical Data Coordinator
Primary RoleDesigns and develops SDTM datasets for clinical trialsManages and oversees data collection and entry in clinical studies
Required SkillsProgramming, SAS, SDTM standardsData management, database systems, regulatory compliance
Work EnvironmentPharmaceutical or CROs, clinical research teamsClinical sites, research organizations, data management teams
CertificationsSAS certifications, knowledge of CDISC standardsData management certifications, possibly SAS or clinical research certifications

The Full Time Sdtm Programmer focuses on creating standardized datasets for analysis, requiring programming skills and SDTM expertise. In contrast, a Clinical Data Coordinator manages data collection and quality control during trials. Both roles are vital in clinical research but differ in technical focus and responsibilities.

How much do entry level clinical SAS programmers make in the US?

Entry-level clinical SAS programmers in the US typically earn between $60,000 and $80,000 annually, depending on location, education, and certifications. Starting salaries may be lower in some regions but tend to increase with experience and proficiency in SAS programming and clinical trial processes.

What is the average salary for a SAS programmer?

The average salary for a SAS programmer varies depending on experience, location, and industry, but typically ranges from $70,000 to $110,000 annually. Full-time SAS programmers with advanced skills in data management and statistical analysis can earn higher salaries, especially in clinical research or pharmaceutical sectors.
More about Full Time Sdtm Programmer jobs
What cities are hiring for Full Time Sdtm Programmer jobs? Cities with the most Full Time Sdtm Programmer job openings:
What are the most commonly searched types of Sdtm Programmer jobs? The most popular types of Sdtm Programmer jobs are:
Infographic showing various Full Time Sdtm Programmer job openings in the United States as of June 2026, with employment types broken down into 4% As Needed, 1% Full Time, 85% Part Time, 1% Temporary, 8% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

Senior Manager, Statistical Programming

BioNTech SE

Gaithersburg, MD โ€ข On-site

$130K - $209K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago


Job description

Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 11351
About the Role
As a Senior Manager, Statistical Programming at BioNTech, you will be instrumental in ensuring high-quality statistical programming deliverables that support our clinical development projects. Working collaboratively with Clinical Development teams or CROs, you will oversee the creation and validation of programming outputs for study reports and regulatory submissions. Your expertise will drive process efficiencies, uphold quality standards, and contribute to the development of global programming tools and standards. Join us to help advance groundbreaking therapies in oncology and infectious diseases.
Your Contribution
  • Collaborate with Clinical Development teams or CROs to meet project timelines for statistical data analysis and reporting
  • Oversee or independently produce and validate programming deliverables such as analysis datasets, tables, listings, and figures
  • Anticipate resource needs and coordinate with management to ensure long-term resource allocation for therapeutic projects
  • Ensure quality control (QC) is performed on all derived datasets, tables, listings, and figures in alignment with company standards and regulatory requirements
  • Participate in developing global programming standards to enable consistent deliverables across portfolios; create tools supporting SDTM/ADaM dataset generation and TLF production
  • Provide functional expertise in establishing BioNTech's centralized clinical data repository, clinical data dictionary, and operational data dictionary
  • Collaborate with Biostatistics to develop statistical applications such as data review and reporting tools
  • Support regulatory submissions by preparing data submission packages including define.xml

A Good Match
  • BSc in Statistics, Mathematics, Computer Science, or related discipline; advanced degree preferred
  • 5+ years (3+ years with advanced degree) experience in pharmaceutical industry/CRO/clinical research settings
  • Strong competence in statistical programming (e.g., SAS/Base, Macro, STAT, GRAPH, SQL)
  • Solid knowledge of FDA/EMA/ICH regulations and guidelines governing clinical trials
  • Familiarity with industry standards for clinical study data reporting (e.g., CDISC standards)
  • Experience in oncology therapeutic area; submission experience preferred
  • Project management skills with strong organizational abilities and attention to detail
  • Excellent communication skills (written/spoken English) with a proactive mindset for problem-solving
  • Ability to thrive in a fast-paced team environment while maintaining analytical rigor

Your benefits and remuneration:
Expected Pay Range: $130,800/year to $209,400/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.
BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:
  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

...and more! More details to be shared.
Apply now - We look forward to your application!
Apply for our Cambridge, US; Gaithersburg, US; New Jersey, US location and simply send us your documents using our online form.
By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.
Inspired? Become part of #TeamBioNTech.
BioNTech, the story
At BioNTech, we are more than just a biotechnology company - we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.
Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.
Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.
BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!
BioNTech - As unique as you
www.biontech.com