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Junior Statistical Programmer Jobs (NOW HIRING)

MMS

Principal Biostatistician - Remote

Phoenix, AZ · On-site

Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments. * High technical level, Subject Matter Expert in biostatistics; willing to guide ...

MMS

Principal Biostatistician - Remote

Canton, MI · On-site

Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments. * High technical level, Subject Matter Expert in biostatistics; willing to guide ...

MMS

Principal Biostatistician - Remote

Raleigh, NC · On-site

Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments. * High technical level, Subject Matter Expert in biostatistics; willing to guide ...

MMS

Principal Biostatistician - Remote

Bridgeport, CT · On-site

Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments. * High technical level, Subject Matter Expert in biostatistics; willing to guide ...

Prometrika LLC

Principal Biostatistician

Cambridge, MA · On-site

$178K - $216K/yr

Provide training and guidance to junior level and new staff * Understand regulatory requirements ... Proficiency in SAS statistical programming * Knowledge of other statistical and data management ...

Caidya

Principal Biostatistician

Morrisville, NC · On-site

Willingness to share expertise with junior staff members. Capabilities * Excellent broad ranging understanding of statistical methods and issues. Demonstrates leadership in several areas of ...

ImmunityBio, Inc.

Principal Biostatistician

Train junior staff in more complex statistical methodology. * Create, edit and adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates. * Performs ad ...

MIT Lincoln Laboratory

D in electrical engineering, computer science, or another relevant discipline or a MS with 5 or ... and mentoring junior staff. * Stakeholder communication - strong written and oral skills for ...

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How much do junior statistical programmer jobs pay per hour?

As of May 29, 2026, the average hourly pay for junior statistical programmer in the United States is $26.96, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $33.17 per hour, depending on experience, location, and employer.

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

To thrive as a Junior Statistical Programmer, you need a solid foundation in statistics, data analysis, and programming skills—often supported by a degree in mathematics, statistics, or a related field. Familiarity with statistical software such as SAS or R and knowledge of data management systems are typically required, with certifications in these tools being advantageous. Attention to detail, problem-solving, and effective communication help you stand out in this role. These skills and qualities are crucial for ensuring accurate data analysis, clear reporting, and successful collaboration within research or clinical trial teams.

What types of projects and tasks can a Junior Statistical Programmer expect to work on in their first year?

As a Junior Statistical Programmer, you will typically work on tasks such as cleaning and organizing datasets, writing basic statistical programming code (often in SAS or R), and assisting in the preparation of tables, listings, and figures for clinical trial reports. You may also support more senior programmers by validating code, performing quality checks, and helping to document programming processes. These responsibilities provide excellent hands-on experience with real-world data and allow you to gradually take on more complex projects as you build your skills and confidence.

What does a Junior Statistical Programmer do?

A Junior Statistical Programmer assists in the analysis and management of clinical trial data using statistical software such as SAS or R. They work under the guidance of senior programmers and statisticians to create, validate, and maintain datasets, generate tables, listings, and figures, and ensure data accuracy and integrity. Their role is crucial in supporting research and regulatory submissions in industries like pharmaceuticals and healthcare.

What is the difference between Junior Statistical Programmer vs Statistical Programmer?

AspectJunior Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some experience or internshipBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supervised tasks, learning on the jobMore independent, handling complex analyses and projects
Employer & Industry UsagePharmaceuticals, biotech, clinical research organizationsSame industries, with increased responsibilities

The main difference between a Junior Statistical Programmer and a Statistical Programmer lies in experience and responsibility. Junior roles focus on learning and supporting tasks, while Statistical Programmers handle more complex analyses independently. Both roles are common in clinical research and biotech industries, with progression often leading from junior to senior positions.

What cities are hiring for Junior Statistical Programmer jobs? Cities with the most Junior Statistical Programmer job openings:
What are the most commonly searched types of Statistical Programmer jobs? The most popular types of Statistical Programmer jobs are:
What states have the most Junior Statistical Programmer jobs? States with the most job openings for Junior Statistical Programmer jobs include:
Junior Statistical Programmer jobs near you
Infographic showing various Junior Statistical Programmer job openings in the United States as of May 2026, with employment types broken down into 95% Full Time, 4% Part Time, and 1% Contract. Highlights an 90% Physical, and 10% Remote job distribution, with an average salary of $56,068 per year, or $27 per hour.
Principal Biostatistician - Remote

Principal Biostatistician - Remote

MMS Holdings Inc.

Remote

Full-time

Posted 15 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Roles and Responsibilities
  • Lead complex projects, programs and submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsors.
  • Can develop SAPs and iSAPs text and shells with no supervision.
  • Produce and present external company presentations providing industry visibility for the organization; Continually suggesting solutions to solve issues in tune with organizational direction.
  • Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments.
  • High technical level, Subject Matter Expert in biostatistics; willing to guide others in a variety of biostatistical techniques.
  • Has the ability to apply drug development knowledge during production of complex statistical analyses.
  • Review or create the statistical section(s) of a Sponsor's protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives. Provide valuable feedback to the Sponsor on the statistical aspects of the study.
  • Prepare and review statistical methods and results sections for the CSR independently in collaboration with in-house medical writers.
  • Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation/management.
  • Perform sample size calculations for a variety of scenarios and study designs. Can provide statistical consulting support to sponsors re study design and sample size calculations.
  • Ability to create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams.
  • Understand the various tools that we work with and able to use them correctly (for SCM: checks in/out; use of external SharePoint).
  • Provide support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
  • Is familiar with and stays current with the latest industry practices and updated regulatory guidelines.
  • Write blogs and/or white papers for posting on the company website.

Requirements
  • Masters in Biostatistics, Statistics discipline or related field, or related experience, PhD preferred.
  • Minimum of 7 years' experience in Biostatistics, Statistics or similar field required.
  • Submission experience (ISS/ISE).
  • Has high level knowledge of drug development as it pertains to biostatistics.
  • Expert knowledge of scientific principles and concepts.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Good organizational skills.
  • High proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Excellent problem-solving skills.
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Good understanding of CROs and scientific & clinical data/terminology, & the drug development process.

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