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Statistical Programmer Ii Jobs (NOW HIRING)

Ensure the statistical programming processes and deliverables are aligned with regulatory ... On-site in Boston (recommended 2-3 days hybrid) or 100% remote with occasional travel to Boston ...

Sr Manager, Statistical Programming

Boston, MA · On-site +1

$151K - $172K/yr

Ensure the statistical programming processes and deliverables are aligned with regulatory ... On-site in Boston (recommended 2-3 days hybrid) or 100% remote with occasional travel to Boston ...

... analysis * 2+ years SAS Base programming using SAS STAT, GRAPH and MACRO * 2+ years relevant ... experience from industry, on clinical trial and clinical database. * CDISC and/or submissions ...

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Statistical Programmer Ii information

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$84.5K

$147.3K

$249K

How much do statistical programmer ii jobs pay per year?

As of Aug 12, 2026, the average yearly pay for statistical programmer ii 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 ii?

A Statistical Programmer II typically requires strong programming skills in SAS or R, experience with clinical trial data, and a relevant degree in statistics, mathematics, or computer science. Familiarity with CDISC standards, data management systems, and regulatory submission requirements is often expected. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for collaborating with cross-functional teams and ensuring data integrity. These competencies help deliver accurate analyses and support regulatory compliance in clinical research environments.

What are some common challenges faced by a statistical programmer ii when collaborating with clinical project teams?

As a Statistical Programmer II, one common challenge is aligning the programming deliverables with the evolving needs of clinical project teams, especially when study protocols or analysis plans change. Effective communication is essential to clarify requirements and timelines with statisticians, data managers, and clinical researchers. Additionally, ensuring data quality and consistency across multiple studies while adhering to regulatory standards can be demanding. Proactively addressing these challenges with strong collaboration and attention to detail helps ensure successful project outcomes.

What is a statistical programmer ii?

Statistical Programmer IIs are professionals who use specialized software to analyze and manage large datasets, typically in clinical research or pharmaceutical settings. They are responsible for programming and validating statistical analyses, generating tables, listings, and figures, and ensuring data accuracy for regulatory submissions. This role requires proficiency in programming languages such as SAS or R, strong analytical skills, and a good understanding of clinical trial processes. Statistical Programmer IIs often work as part of a team, collaborating with statisticians and data managers to deliver high-quality data outputs.

What is the difference between Statistical Programmer Ii vs Data Analyst?

AspectStatistical Programmer IiData Analyst
Required CredentialsBachelor's in Statistics, Computer Science, or related field; programming skills in SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical or clinical research settings, working with clinical trial dataBusiness, healthcare, or marketing sectors analyzing large datasets
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsCorporations, healthcare providers, market research firms

While both roles involve data analysis, Statistical Programmer Ii primarily focuses on programming and preparing clinical trial data, whereas Data Analysts interpret data to inform business decisions. The roles share similar educational backgrounds and technical skills but differ in industry focus and daily tasks.

More about Statistical Programmer Ii jobs
What cities are hiring for Statistical Programmer Ii jobs? Cities with the most Statistical Programmer Ii job openings:
What states have the most Statistical Programmer Ii jobs? States with the most job openings for Statistical Programmer Ii jobs include:
Infographic showing various Statistical Programmer Ii job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $147,292 per year, or $70.8 per hour.

Principal Statistical Programmer

Pharpoint Research

Durham, NC • On-site

Full-time

Re-posted 25 days ago


Job description

Description:

BASIC SUMMARY:

Provide overall technical, administrative and functional oversight for the programming activities supporting biostatistics which include the development of analysis datasets, and statistical summaries. Oversee the efficient, accurate, and timely execution of all programming activities within biostatistics. Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs) set forth by PharPoint Research, Inc. and its sponsor clients.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Efficiently and effectively coordinate statistical programming activities for at least 4 projects simultaneously which could be satisfied by 4 separate protocols, a program consisting of at least 2 separate compounds with multiple studies per compound, or NDA submission.
  • Plan and coordinate processes to ensure quality and efficient programming, verification, and documentation of programs for use in creating clinical databases, analysis datasets, tables, listings, and figures.
  • Provide senior level oversight for departmental teams.
  • Ensure the efficiency, quality, and integrity of analyses, data reporting, project, and supervisory activities executed.
  • Successfully represent the department and the company in client meetings/presentations and maintain a positive working relationship with sponsors, regulatory agencies, collaborating associates, vendor personnel and subcontract personnel.
  • Facilitate advanced technical expertise, in conjunction with internal and external team members, to design, implement, validate, and maintain project reporting applications that are supported by the department.
  • Identify project priorities and project timeline goals and communicate priority-related issues and timelines to programming teams.
  • Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
  • Efficiently manage project budgets to identify resourcing or scope of work changes.
  • Provide accurate and timely project status updates to other team members, colleagues, and senior management.
  • Serve as a model to departmental subordinates as it relates to effective time management, communication, and utilization of resources. Provide leadership and motivation to departmental personnel.
  • Contribute to ongoing improvement of programming processes and methodology.
  • Provide senior leadership and guidance to departmental employees to ensure accuracy and adherence to pertinent departmental policies, practices, and procedures.
  • Manage activities of assigned project team(s) to ensure effective performance of a clinical trial program. Provide direction to team members working toward a common goal and successfully coordinate multiple priorities.
  • Interact collaboratively with staff across departments to ensure that project and departmental activities are successfully completed.
  • May participate in the interview and selection of qualified personnel.
  • Assist in the development, implementation, and delivery of departmental training programs; server as a mentor to junior level programmers.
  • May attend related continuing education programs, professional meetings, and/or company career development activities sponsored or approved by the company.
  • Assist in the development, maintenance, and communication of departmental systems and SOPs.
  • Perform all other related duties as assigned.


Requirements:

QUALIFICATIONS:

  • Education: Bachelor’s degree (B.A./B.S.) or equivalent in Statistics, Computer Science or related field.
  • Experience: 9 years relevant experience in clinical research. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Certification/Licensure: None
  • Other: Effective team player: willingness to go the extra distance to get results, meet deadlines, etc. Able to manage many projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change. Strong ability to motivate staff within project teams and ensure productivity and smooth operation in conditions with ambiguity. Leadership skills in priority evaluations, adapting to changes, conflicts resolutions, and effective partnership. Knowledge of one or more statistical software packages used to conduct statistical analyses required. Ability to read, write, speak, and understand English required.


PHYSICAL DEMANDS:

  • While performing the duties of this job, the employee is regularly required to talk, hear, and type at a computer.
  • Specific vision abilities required by this job include close vision and the ability to adjust focus.


WORK ENVIRONMENT:

  • General office working conditions, the noise level in the work environment is usually quiet.


COMMENTS:

  • This position may require occasional domestic/international travel.
  • Must have a valid driver’s license with no limitations on driving availability.