1

Statistical Programmer 2 Jobs (NOW HIRING)

Ensure the statistical programming processes and deliverables are aligned with regulatory ... Some domestic and international travel required (2-3 times per year) * On-site in Boston ...

New

OR · On-site

$153K - $199K/yr

Statistical programmers work collaboratively with internal colleagues and external vendors to ... PhD degree in Biostatistics/Computer Sciences or equivalent 2+ years of experience in pharma ...

OR · On-site

$153K - $199K/yr

Statistical programmers work collaboratively with internal colleagues and external vendors to ... PhD degree in Biostatistics/Computer Sciences or equivalent 2+ years of experience in pharma ...

Basic Qualifications: • Doctorate degree OR • Master's degree and 2 years of statistical programming experience OR • Bachelor's degree and 4 years of statistical programming experience OR • ...

The Computer Programmer II provides mid-level software development and maintenance support for the National Vital Statistics System (NVSS), National Death Index (NDI), and related CDC/NCHS DVS ...

next page

Showing results 1-20

Statistical Programmer 2 information

See salary details

$84.5K

$147.3K

$249K

How much do statistical programmer 2 jobs pay per year?

As of Jun 5, 2026, the average yearly pay for statistical programmer 2 in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Statistical Programmer 2, and why are they important?

To thrive as a Statistical Programmer 2, you need a strong background in statistics, data analysis, and programming languages such as SAS or R, usually supported by a degree in statistics, mathematics, or a related field. Experience with clinical trial data standards (like CDISC SDTM/ADaM), regulatory submission requirements, and data management systems is typically expected. Attention to detail, strong problem-solving skills, and effective communication are essential soft skills that help ensure accuracy and collaboration. These competencies are vital for delivering reliable statistical outputs and supporting successful clinical research and regulatory submissions.

How does a Statistical Programmer 2 typically collaborate with biostatisticians and clinical teams during a clinical trial project?

As a Statistical Programmer 2, you will frequently work closely with biostatisticians to implement statistical analysis plans, ensuring that data outputs meet regulatory standards and project specifications. Collaboration with clinical teams is also essential for clarifying data requirements, resolving discrepancies, and understanding study protocols. Effective communication and teamwork are crucial, as you may be responsible for translating statistical methods into programming code and explaining technical outputs to non-programmers. This collaborative environment provides opportunities to expand both your technical and interpersonal skills.

What are Statistical Programmer 2s?

A Statistical Programmer 2 is a mid-level professional who specializes in writing and managing computer programs to analyze and process data, often in clinical research or pharmaceutical settings. They are responsible for generating statistical tables, listings, and figures, as well as validating data and ensuring compliance with regulatory standards. Typically, they work with software like SAS or R and collaborate closely with statisticians, data managers, and clinical teams to support data-driven decision-making. Their role requires a solid understanding of statistical methodologies, programming skills, and industry regulations.
More about Statistical Programmer 2 jobs
What job categories do people searching Statistical Programmer 2 jobs look for? The top searched job categories for Statistical Programmer 2 jobs are:
Infographic showing various Statistical Programmer 2 job openings in the United States as of May 2026, with employment types broken down into 99% Full Time, and 1% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $147,292 per year, or $70.8 per hour.
Sr. Principal Analyst, Statistical Programming

Sr. Principal Analyst, Statistical Programming

Neurocrine Biosciences

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago


Job description

Who We Are:

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.

What We Do:

Neurocrine Biosciencesis a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visitneurocrine.com, and follow the company onLinkedIn,XandFacebook. (*in collaboration with AbbVie)

About the Role:Leads major statistical programming efforts for clinical program area of responsibility. Develops and recommends system capabilities roadmap for in-house development and external vendor selection process. Acts as a system expert in designing, developing, testing, maintaining, validating, and documenting SAS programs to evaluate clinical data and meet the project requirements for SAS statistical programming efforts. Provides expert-level technical advice for all aspects of the program development process, tools and software, standards and procedures.

_

Your Contributions (include, but are not limited to):
  • Provides expert technical leadership across multiple functions serving as the key representative for Biometrics

  • Contributes to the development of Biometrics functional strategy and serves as system expert for Statistical Programming efforts

  • Leads and mentors a team of statistical programmers to support the analysis and reporting of data from clinical and nonclinical studies for all corporate development programs

  • Leads end-to-end statistical programming work-streams on multidisciplinary program teams company-wide

  • Provides technical direction in the development and implementation of programming standards and conventions, building statistical programming infrastructure

  • Provides workforce planning recommendations based on project workloads in order to ensure appropriate programming resources are available to complete tasks in a timely manner

  • Manages vendor selection processes and validates vendor programming activities such as CDISC implementation, analysis reporting, and programming conventions

  • Supports creation and validation of e-submission requirements (i.e. annotated CRF, datasets files, define documents)

  • Serves as primary/lead programmer for agency reporting deliverables such as DSUR/Annual Report and IB updates

  • Performs the function of lead and/or quality control statistical programmer on projects as needed

  • Performs other duties as assigned

Requirements:
  • BS/BA degree in computer science, mathematics, statistics, or related discipline AND 8+ years in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity. Experience managing large projects and external vendors. OR

  • Master's degree in computer science, mathematics, statistics, or related discipline AND 6+ years similar experience noted above OR

  • PhD degree in computer science, mathematics, statistics, or related discipline AND 4+ years similar experience noted above

  • Anticipates business and industry issues; recommends relevant process / technical / service improvements

  • Demonstrates broad expertise or unique knowledge

  • Considered an expert within the company and may have external presence in area of expertise

  • Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency of team

  • Ability to work as part of and lead multiple teams

  • Good leadership, mentoring skills and abilities typically leads lower levels and/or indirect teams

  • Excellent computer skills

  • Excellent communications, problem-solving, analytical thinking skills

  • Sees broader picture and longer-term impact on division/company

  • Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency

  • Excellent project management, strong project leadership skills

  • Expert knowledge of the following:

    • Developing and implementing statistical programming SOPs and processes in a clinical environment

    • Relational databases and complex data systems.

    • Industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines

    • Programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar

    • SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains

  • Knowledge of all aspects of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems

  • Proven experience in multi-discipline, cross-functional project management in a clinical, highly regulated environment

  • Track record of success with effectively organizing and managing multiple assignments with challenging timelines across multiple personnel

#LI_SA1

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.

_

The annual base salary we reasonably expect to pay is $156,900.00-$214,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.