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Associate Director Statistical Programming Jobs in Wayne, PA

MSD

Assoc. Dir , D&A Strategy

North Wales, PA · On-site

Associate Director - Data Strategy, Oncology This role will reside within the Digital Human Health ... Statistics, Decision Science, Marketing, Engineering, or Public Health is required. * MBA, MS or ...

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All JobsAssociate Statistical Programming JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Wayne, PA

Associate Director Statistical Programming information

See Wayne, PA salary details

$139.1K

$253.9K

$311.7K

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

As of Aug 13, 2026, the average yearly pay for associate director statistical programming in Wayne, PA is $253,862.00, according to ZipRecruiter salary data. Most workers in this role earn between $236,100.00 and $292,200.00 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 Wayne, PA?

For Associate Director Statistical Programming jobs in Wayne, PA, the most frequently searched job titles are:

What job categories do people searching Associate Director Statistical Programming jobs in Wayne, PA look for?

The top searched job categories for Associate Director Statistical Programming jobs in Wayne, PA are:

What cities near Wayne, PA are hiring for Associate Director Statistical Programming jobs?

Cities near Wayne, PA 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 Wayne, PA 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 $253,862 per year, or $122 per hour.

Senior Director, Biostatistics

Uniquity Bio

Malvern, PA • Remote

Full-time

Re-posted 12 days ago

Job description

Uniquity Bio is a clinical-stage biotechnology company committed to putting science and patients first. We exist to develop transformative new medicines for immune-mediated diseases, and we’re looking for bright-minded professionals driven by a desire to advance science and make a difference for people in need. Our lead asset, solrikitug, is a highly-potent TSLP inhibitor now in Phase 2 clinical trials for asthma, chronic obstructive pulmonary disease (COPD), and eosinophilic esophagitis (EoE) indications.

Join us in building an organization where people and science thrive together. You’ll have the opportunity to make a meaningful impact while working alongside a talented, agile team in an environment where ideas move quickly, colleagues are trusted, and quality remains a cornerstone.

Position Overview

Uniquity Bio is seeking an experienced and strategic Senior Director, Biostatistics to provide statistical leadership across one or more clinical development programs within a fast-paced and highly collaborative environment. This individual will serve as a key cross-functional partner to Clinical Development, Clinical Operations, Data Management, Statistical Programming, Medical Writing, Regulatory Affairs, and external partners to support the design, analysis, interpretation, and reporting of clinical studies.

The Senior Director will play a critical role in advancing programs from early development through late-stage clinical execution and regulatory submission activities. The ideal candidate combines strong technical expertise with strategic thinking, operational excellence, and the ability to influence across multidisciplinary teams.

This role requires a hands-on leader who is comfortable operating both strategically and tactically within a growing biotechnology organization.


Key Responsibilities

  • Provide statistical leadership and strategic guidance across one or more clinical development programs from protocol concept through regulatory submission and post-hoc analyses
  • Lead statistical contributions to study design, including endpoint strategy, estimands, randomization methodology, multiplicity adjustments, interim analyses, and sample size determination
  • Author, review, and approve statistical sections of protocols, statistical analysis plans (SAPs), clinical study reports (CSRs), regulatory briefing documents, publications, and other study-related deliverables
  • Oversee development, validation, and review of statistical outputs, tables, listings, and figures to ensure quality, reproducibility, traceability, and regulatory compliance
  • Ensure statistical analyses and deliverables meet internal quality standards as well as applicable regulatory expectations and industry best practices
  • Partner closely with cross-functional study teams to support data review, interpretation of study results, risk assessment, and decision-making throughout the clinical development lifecycle
  • Lead and manage relationships with external CROs, biostatistics vendors, and programming partners, including scope definition, timelines, budget oversight, quality management, and performance monitoring
  • Support global regulatory interactions, including preparation for Health Authority meetings, submission activities, and responses to regulatory questions
  • Contribute to the development and implementation of departmental standards, processes, statistical methodologies, and operational best practices
  • Hire, mentor, coach, and develop biostatistics talent as the organization continues to scale
  • Serve as a strategic thought partner to senior leadership and contribute to broader organizational and portfolio-level initiatives


Qualifications

  • PhD or MS in Biostatistics, Statistics, or related quantitative field with significant industry experience in biotechnology or pharmaceutical drug development
  • Typically 12+ years of relevant biostatistics experience within the pharmaceutical, biotechnology, or CRO industry, including leadership responsibility supporting clinical development programs
  • Demonstrated experience supporting clinical studies across multiple phases of development, including late-stage studies and regulatory submissions
  • Deep understanding of clinical trial methodology, statistical principles, regulatory guidance, and industry standards applicable to drug development
  • Strong experience authoring and reviewing SAPs, protocols, CSRs, and regulatory submission documents
  • Hands-on experience with statistical programming environments such as R and/or SAS, including review of analysis code and outputs
  • Proven ability to effectively manage external vendors and CRO partners within a matrixed development environment
  • Experience participating in Health Authority interactions and supporting global submissions strongly preferred
  • Excellent communication, collaboration, and influencing skills with the ability to communicate complex statistical concepts to both technical and non-technical audiences
  • Demonstrated success operating in a fast-paced, highly collaborative biotech environment with evolving priorities
  • Prior people management and team development experience preferred


Work Environment


At Uniquity Bio, we believe every team member has an impact on the patients we aim to serve. We are a nimble team with a rigorous approach to drug development that requires collaboration and transparency to maximize value, reduce risk, and deliver meaningful, best-in-class products. We are looking for self-starters who enjoy working in a complex, collaborative environment and are motivated to bring critical new medicines to people around the world. We are a small, fast-paced organization with a talented team of in-house employees and external consultants. Candidates must be self-motivated and able to work both independently and collaboratively to achieve success and impact in our dynamic work environment.

This is a U.S.-based position. Team members who live within commuting distance of our Malvern, PA or San Diego, CA office locations are expected to spend time in the office, and remote employees are expected to travel to an office on a regular basis. Specific details for both local and remote staff will be discussed and agreed upon on a case-by-case basis with the employee’s manager. Business travel may be required depending upon the specific needs of the position.

The above job description is not intended to be all-inclusive. Requirements of the position may change from time to time based on business needs.


Uniquity Bio is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.