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Director Statistical Programming Jobs in Bristol, CT

micro1 AI

Director of Biostatistics

Waterbury, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Hartford, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

New Haven, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

New Haven, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Hartford, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Waterbury, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Kemper

Data Science Manager

Hartford, CT · Hybrid

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Our success is a direct reflection of the talented and diverse people who make a positive ... PhD in Mathematics, Statistics, Engineering, or other STEM fields preferred with 4-6 years of ...

IDEX

Director of Process Engineering

Farmington, CT · On-site

  • Medical

  • Retirement

  • PTO

The Director of Process Engineering is responsible for leading the development, optimization, and ... Cpk) Statistical process control where applicable; drives repeatability Cycle Time Reduction ...

Ametek

Manufacturing Quality Engineer

Middlefield, CT · On-site

$72K - $93K/yr

  • Retirement

  • PTO

Use statistical analysis, process capability studies, trend analysis, and other data-driven tools ... Optical Engineering preferred. * 3-8 years of direct Quality Engineering experience in a ...

Ametek

Manufacturing Quality Engineer

Middlefield, CT · On-site

$72K - $93K/yr

  • Retirement

  • PTO

Use statistical analysis, process capability studies, trend analysis, and other data-driven tools ... Optical Engineering preferred. * 3-8 years of direct Quality Engineering experience in a ...

IDEX

Director of Process Engineering

Farmington, CT · On-site

$158.60 - $237.80/hr

  • Medical

  • Retirement

  • PTO

The Director of Process Engineering leads the development, optimization, and scale‑up of ... Process Capability (Cp/Cpk) and statistical process control. * Cycle time reduction and throughput ...

Kamis

Quality Engineer

Torrington, CT

$71K - $91K/yr

Substitutes in the absence of the QA Director. Qualifications Thorough knowledge of quality ... Excellent math skills and understanding of Statistics as they apply to measurement. Good written ...

Connecticut Spring & Stamping

Quality Engineer

Farmington, CT · On-site

$76K - $98K/yr

Requires direct experience working in a metal form/metal stamping industry. * Works with Operations ... Perform statistical techniques as needed, including SPC * Determine inspection methods Lean ...

The Hartford

Director of Data Science

Hartford, CT · On-site +1

$153K - $229K/yr

Partner with Actuarial, Data Engineering, and other modeling organization teams to connect modeling ... D. in Statistics, Applied Mathematics, Quantitative Economics, Actuarial Science, Data Science ...

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All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Bristol, CT

Director Statistical Programming information

See Bristol, CT salary details

$153.7K

$280.5K

$344.5K

How much do director statistical programming jobs pay per year?

As of Aug 13, 2026, the average yearly pay for director statistical programming in Bristol, CT is $280,522.00, according to ZipRecruiter salary data. Most workers in this role earn between $260,800.00 and $322,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
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Director Statistical Programming jobs near you

Director of Biostatistics

micro1 AI

Waterbury, CT • Remote

$60 - $65/hr

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks that require deriving, reproducing, or validating statistical outputs from clinical datasets and associated tables, figures, and listings (TFLs).
  2. Apply expert judgment to assess the correctness and consistency of reported estimates, confidence intervals, p-values, analysis populations, and missing data handling in alignment with the statistical analysis plan (SAP).
  3. Identify discrepancies between statistical outputs and their narrative descriptions in clinical study reports (CSR), including subtle errors in population definitions, censoring rules, or multiplicity handling.
  4. Establish defensible ground truth for each evaluation task, documenting the derivation process to enable independent verification.
  5. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives, employing clear and concise communication.
  6. Collaborate with a multidisciplinary project team, providing statistical insights and feedback as needed to refine evaluation tasks and criteria.


Preferred Qualifications

  1. 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit.
  2. Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets.
  3. Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies under ICH E9(R1).
  4. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications.
  5. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses.
  6. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field.
  7. Nice to have: Experience as lead statistician on pivotal/registrational studies, authoring or reviewing CSR statistical sections, oncology endpoint expertise, and exposure to AI-assisted statistical review tools.

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