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Remote Director Statistical Programming Jobs in Philadelphia, PA

Slipstream IT

Statistical Analytical Programmer

PA · On-site +1

Able to work independently in a remote environment and manage timelines effectively. Preferred Qualifications: * Experience with R for data analysis, programming, or statistical workflows is highly ...

TechData Service Company LLC

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Remote Statistician-Real World Evidence (RWE)

King Of Prussia, PA · Remote

$100K - $160K/yr

... statistical programming languages/software such as SAS and/or R · Able to work in a virtual environment · Teamwork and leadership skills · Technical expertise and application with working ...

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All JobsStatistical Programming JobsRemote Director Statistical Programming JobsRemote Director Statistical Programming Jobs in Philadelphia, PA

Remote Director Statistical Programming information

See Philadelphia, PA salary details

$154.9K

$282.7K

$347.1K

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

As of Aug 29, 2026, the average yearly pay for remote director statistical programming in Philadelphia, PA is $282,693.00, according to ZipRecruiter salary data. Most workers in this role earn between $262,900.00 and $325,400.00 per year, depending on experience, location, and employer.

What is a remote director statistical programming?

A Remote Director of Statistical Programming is a senior-level professional who oversees statistical programming teams and projects, often within the pharmaceutical, biotechnology, or clinical research industries, while working remotely. They are responsible for ensuring the accuracy and efficiency of statistical data analysis and reporting, particularly for clinical trials and regulatory submissions. This role involves managing programmers, developing programming standards, ensuring compliance with regulatory requirements, and collaborating closely with statisticians, data managers, and project leaders. Working remotely, they utilize digital tools to lead distributed teams and maintain high-quality data deliverables. Their work is critical in transforming raw clinical data into meaningful insights for decision-making and regulatory approval.

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

To thrive as a Remote Director Statistical Programming, you need advanced expertise in statistical programming (typically SAS and R), a strong background in biostatistics or related fields, and significant experience in clinical trial data analysis, usually supported by a relevant degree. Mastery of programming tools, regulatory submission standards (such as CDISC SDTM/ADaM), and familiarity with data management systems are crucial, along with relevant certifications being advantageous. Leadership, strategic thinking, and exceptional communication skills help you effectively manage teams and collaborate across global, cross-functional groups. These skills ensure accurate, regulatory-compliant analyses that drive successful clinical development and organizational goals.

How does a remote director statistical programming typically collaborate with cross-functional teams while managing geographically dispersed staff?

A Remote Director of Statistical Programming often leads a team of programmers who may be distributed across different locations and time zones. Collaboration with cross-functional teams—such as biostatisticians, data managers, and clinical operations—relies heavily on clear communication through virtual meetings, shared project management tools, and regular status updates. The director is responsible for aligning programming deliverables with project timelines, ensuring quality standards, and fostering a cohesive team environment despite the remote setup. Strong leadership and proactive engagement are essential to overcome challenges like time zone differences and maintain alignment with overall project goals.

What is the difference between Remote Director Statistical Programming vs Remote Statistical Programming Manager?

AspectRemote Director Statistical ProgrammingRemote Statistical Programming Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and extensive experienceRequires similar degrees and experience, but slightly less senior
Work EnvironmentLeadership role overseeing multiple teams, strategic planningManages teams directly, focuses on project execution
Industry UsageCommon in large pharma and biotech companiesFound in similar settings, often as a mid-level leadership role
Search & Comparison IntentOften searched by senior professionals or recruitersMore frequently searched by mid-level managers or job seekers

The Remote Director Statistical Programming is a senior leadership role overseeing multiple teams and strategic initiatives, requiring extensive experience and advanced degrees. In contrast, the Remote Statistical Programming Manager focuses on managing project teams and day-to-day operations. Both roles are vital in pharmaceutical and biotech industries, but they differ mainly in seniority and scope of responsibilities.

What are popular job titles related to Remote Director Statistical Programming jobs in Philadelphia, PA?

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

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

The top searched job categories for Remote Director Statistical Programming jobs in Philadelphia, PA are:

Remote Director Statistical Programming jobs near you

Senior Director, Head of Statistical Programming

Malvern, PA • Remote

Uniquity Bio
See more jobs at Uniquity Bioexternal

Full-time

Re-posted 27 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 a highly experienced and strategic Senior Director, Head of Statistical Programming to lead and scale the Statistical Programming function within our growing Biostatistics and Data Sciences organization. This individual will provide both strategic and operational leadership across clinical development programs and will be responsible for the delivery, quality, and integrity of statistical programming outputs supporting clinical trials, regulatory submissions, publications, and internal decision-making.

The Senior Director will play a critical role in establishing programming standards, building scalable infrastructure, and driving operational excellence across all programming activities. This position requires deep technical expertise, strong leadership capabilities, and the ability to collaborate effectively within a dynamic, cross-functional biotechnology environment.

The ideal candidate is a hands-on leader with extensive experience supporting regulatory submissions, managing external vendors and CROs, and building high-performing programming organizations within a fast-paced clinical-stage biotech setting. 



Key Responsibilities

  • Define and lead the vision, standards, operational strategy, and long-term scalability roadmap for the Statistical Programming function
  • Build, mentor, and develop internal statistical programming capabilities through strategic hiring, coaching, resource planning, and team leadership
  • Oversee the development, validation, review, and delivery of SDTM datasets, ADaM datasets, tables, listings, figures (TLFs), and related programming deliverables across clinical development programs
  • Ensure all programming deliverables meet internal quality standards, CDISC compliance requirements, and applicable regulatory expectations for global submissions
  • Provide technical and operational oversight for programming activities supporting clinical trials, regulatory submissions, publications, safety analyses, and ad hoc data requests
  • Drive programming strategy and readiness for regulatory interactions and submissions, including FDA, EMA, PMDA, NDA, BLA, and MAA activities
  • Establish, maintain, and optimize programming processes, standards, SOPs, macros, validation frameworks, and data governance workflows to improve consistency, efficiency, scalability, and inspection readiness
  • Lead and oversee relationships with external CROs, statistical programming vendors, and independent contractors, including scope management, quality oversight, timeline accountability, and budget management
  • Partner closely with Biostatistics, Data Management, Clinical Operations, Medical Writing, Regulatory Affairs, and Clinical Development teams to ensure alignment on study timelines, deliverables, and data quality expectations
  • Contribute to submission strategy discussions, inspection readiness activities, and responses to regulatory questions related to programming deliverables and data standards
  • Evaluate and implement innovative technologies, tools, and automation opportunities to enhance programming efficiency and reproducibility
  • Support organizational growth initiatives and contribute to broader departmental strategy and operational planning efforts


Qualifications

  • Bachelor’s, Master’s, or PhD in Statistics, Biostatistics, Computer Science, Mathematics, or related quantitative discipline
  • Typically, 12+ years of statistical programming experience within the biotechnology, pharmaceutical, or CRO industry, including leadership experience supporting clinical development programs
  • Demonstrated experience leading statistical programming activities across multiple phases of clinical development, including late-stage studies and regulatory submissions
  • Deep expertise in CDISC standards, including SDTM and ADaM implementation
  • Expert-level proficiency in SAS required; familiarity with R and/or Python strongly preferred
  • Strong understanding of clinical trial processes, regulatory requirements, and industry best practices related to statistical programming and submission deliverables
  • Proven experience managing external CROs, vendors, and outsourced programming models within a matrixed environment
  • Demonstrated ability to establish scalable programming standards, processes, and operational infrastructure within a growing organization
  • Prior experience supporting FDA, EMA, PMDA, NDA, BLA, and/or MAA submissions strongly preferred
  • Excellent leadership, communication, collaboration, and organizational skills with the ability to influence across cross-functional teams and executive stakeholders
  • Ability to thrive in a fast-paced, highly collaborative, and evolving biotechnology environment


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.



  

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