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Associate Director Statistical Programming Jobs in Rochester, NY

micro1 AI

Director of Biostatistics

Rochester, NY · 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 ...

L3HHCM20

Associate, Quality Engineering

Rochester, NY · On-site

$56K - $104K/yr

Associate, Quality Engineer Job Code: 40221 Job Location: Rochester, NY Job Schedule: 9/80 ... Develop and implement quality processes and procedures using statistical quality control statistics ...

Pwc

Data Engineer - Senior Associate

Rochester, NY · On-site

$77K - $202K/yr

... directed acyclic graphs (DAGs) for efficient data organization and processing - Supporting the ... Statistics - Demonstrating proficiency in data engineering platforms like Databricks - Utilizing ...

L3HHCM20

Associate, Manufacturing Engineer

Rochester, NY · On-site

$5.6K - $10K/mo

Job Title: Associate, Manufacturing Engineer Job Code: 40080 Job Location: Rochestser, NY Job ... Experience with Minitab, JMP, or other statistical software PAY TRANSPARENCY: In compliance with ...

Pwc

Data Engineer - Senior Associate

Rochester, NY · On-site

$77K - $202K/yr

... Statistics - 2 years of experience What Sets You Apart - Certification in Cloud Platforms [e.g ... At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship ...

Pwc

US Tech - AI Engineering Senior Associate

Rochester, NY · On-site

$55K - $187K/yr

You will work on developing predictive models, conducting statistical analysis, and creating data ... At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship ...

Ralliant

Senior Process Engineering

Fairport, NY · On-site

$98K - $127K/yr

Familiarity with statistical methods and software (Minitab, JMP, etc.). * Proficient in database ... with associates throughout the organization. * Organized, self-directed, and able to manage ...

Ralliant

Senior Process Engineering

Fairport, NY · On-site

$98K - $127K/yr

Familiarity with statistical methods and software (Minitab, JMP, etc.). * Proficient in database ... with associates throughout the organization. * Organized, self-directed, and able to manage ...

Ralliant

Manufacturing Process Engineer

Fairport, NY · On-site

$69K - $93K/yr

Familiarity with statistical methods and software (Minitab, JMP, etc.). * Proficient in database ... with associates throughout the organization. * Organized, self-directed, and able to manage ...

Pwc

US Tech - FTO Senior Associate

Rochester, NY · On-site

$55K - $187K/yr

... Engineering, Mathematics/Statistics - Demonstrating proficiency in AWS CloudFormation and Azure ... At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship ...

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All JobsAssociate Statistical Programming JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Rochester, NY

Associate Director Statistical Programming information

See Rochester, NY salary details

$151.5K

$276.4K

$339.4K

How much do associate director statistical programming jobs pay per year?

As of Aug 11, 2026, the average yearly pay for associate director statistical programming in Rochester, NY is $276,413.00, according to ZipRecruiter salary data. Most workers in this role earn between $257,000.00 and $318,200.00 per year, depending on experience, location, and employer.

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

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

What does an associate director statistical programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

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

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in Rochester, NY? For Associate Director Statistical Programming jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Rochester, NY look for? The top searched job categories for Associate Director Statistical Programming jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Associate Director Statistical Programming jobs? Cities near Rochester, NY with the most Associate Director Statistical Programming job openings:
Associate Director Statistical Programming jobs near you
Infographic showing various Associate Director Statistical Programming job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Hybrid job distribution, with an average salary of $276,413 per year, or $132.9 per hour.

Director of Biostatistics

micro1 AI

Rochester, NY • Remote

$60 - $65/hr

Part-time

Posted 7 days ago

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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