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Remote Director Statistical Programming Jobs in Islip, NY

R or Python Statistical Programming, Structured Query Language (SQL), Tableau/Power BI, Snowflake ... and remote work for focused tasks. Inclusivity & Accessibility Altus Group is committed to ...

A real estate services firm in New York City has a great Remote opportunity awaiting a new Data ... Statistical Analysis, Data Engineering and Data Visualization related work * Associate's and/or ...

As a Data Scientist, you will be working with our engineering team to model complex problems and ... Bachelor in Statistics, Mathematics, Computer Science, or related field; graduate degree in Data ...

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Remote Director Statistical Programming information

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$159.1K

$290.4K

$356.5K

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

As of Aug 7, 2026, the average yearly pay for remote director statistical programming in Islip, NY is $290,353.00, according to ZipRecruiter salary data. Most workers in this role earn between $270,000.00 and $334,200.00 per year, depending on experience, location, and employer.

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 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.

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 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 job categories do people searching Remote Director Statistical Programming jobs in Islip, NY look for? The top searched job categories for Remote Director Statistical Programming jobs in Islip, NY are:
What cities near Islip, NY are hiring for Remote Director Statistical Programming jobs? Cities near Islip, NY with the most Remote Director Statistical Programming job openings:

Director, Statistical Programming (Pharma/Biotech Experience Required)

LB Pharmaceuticals

New York, NY • Remote

Full-time

Posted 2 days ago

New


Job description

Salary:

The Director of Statistical Programming is a pivotal, newly created role at LB Pharmaceuticals, reflecting our commitment to building a best-in-class internal Biometrics capability. This individual will serve as the founding leader of our Statistical Programming function, responsible for building the team, infrastructure, and processes from the ground up. The Director will be a hands-on technical leader and strategic partner, working closely with the VP of Biometrics, Biostatistics, Clinical Operations, and Regulatory Affairs to support late-stage clinical trials and BLA submission planning.

Responsibilities

Team & Infrastructure Building

  • Establish and lead the internal Statistical Programming function, defining organizational structure, hiring plans, and resourcing strategy as the company scales toward BLA.
  • Design and implement the programming infrastructure, including SAS/R environments, standard macros, validation frameworks, SDTM/ADaM libraries, and TLF shells aligned with CDISC standards.
  • Develop and maintain SOPs, work instructions, and best practices for all statistical programming activities.
  • Recruit, mentor, and grow a high-performing team of statistical programmers (contractors and FTEs) over time.

Hands-On Programming & Deliverables

  • Serve as lead programmer on CNS clinical trials (schizophrenia, bipolar depression, MDD), including Phase 2 and Phase 3 studies.
  • Develop and validate SDTM and ADaM datasets, TLFs, and supporting documentation for regulatory submissions in full compliance with FDA and ICH guidelines.
  • Lead statistical programming activities for IND/NDA/BLA submissions, including Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), eCTD packaging, Define.xml, Reviewer's Guide, and CDISC compliance checks.
  • Collaborate with Biostatistics to implement statistical analysis plans (SAPs) and provide programming support for ad hoc analyses.

Vendor Oversight & Governance

  • Oversee and manage CRO/vendor statistical programming activities, including scope of work definition, timeline management, quality review, and deliverable acceptance.
  • Establish vendor governance frameworks including quality oversight plans, technical review checklists, and escalation pathways.
  • Ensure vendor-produced datasets, TLFs, and submission packages meet internal and regulatory standards prior to acceptance.

Regulatory & Cross-Functional Collaboration

  • Partner with Regulatory Affairs and Biostatistics to develop and execute the BLA submission strategy and data package planning for LB-102.
  • Liaise with FDA on data standards, submission requirements, and any technical queries related to statistical programming deliverables.
  • Collaborate with Clinical Data Management to ensure alignment on data flow, edit checks, database lock timelines, and data quality.
  • Contribute to Health Authority meetings and respond to regulatory requests related to statistical programming.

Qualifications

  • Bachelors or Masters degree in Statistics, Computer Science, Mathematics, or a related quantitative field.
  • Minimum 10 years of statistical programming experience in the pharmaceutical or biotech industry, with at least 3 years in a leadership or senior role.
  • Demonstrated experience supporting NDA or BLA submissions, including hands-on SDTM/ADaM development and regulatory-grade TLF production.
  • Deep expertise in SAS (Base, Macro, STAT, ODS); proficiency in R is highly desirable.
  • Strong working knowledge of CDISC standards (SDTM, ADaM, SEND, Define.xml) and FDA/ICH submission guidelines (including 21 CFR Part 11).
  • Proven ability to manage and oversee CRO/vendor programming deliverables in a sponsor oversight capacity.
  • Experience in a small or mid-size biotech environment, including comfort with ambiguity and ability to build processes from scratch.
  • Experience in CNS therapeutic areas, particularly schizophrenia, bipolar disorder, or MDD preferred.
  • Familiarity with FDA expectations for CNS endpoint programming (e.g., PANSS, MADRS, YMRS, CGI scales) preferred.
  • Prior experience building or standing up a statistical programming function at a growing biotech preferred. .
  • PharmaSUG, CDISC, or equivalent industry certifications preferred.


The posted salary range reflects the minimum to maximum base pay for this position in the specified location. Actual compensation may vary based on factors such as geographic location, experience, education, licensure requirements, and skill level, and will be determined at the time of offer. Base Salary Range: $226K $240K

The Values We Hope You Share

Purpose Driven We are optimistic, focused and committed to delivering on our vision. We are hard-working, compliant,relentlessand impatient in our pursuit oftreatments. We set competitive company goals to significantly and positivelyimpactthe lives of our patients,employeesand shareholders. We have a sense of urgencytoevery action wemake.

Transparent We trust each other and expect honest and open communication to enable good decision making. We are humble,genuineand direct. Words match ourbehaviors. We hold each other accountable. We embracethe toughconversations to achieve success.

Bold We are courageous in our pursuit of excellence. Unafraid of risks. Unafraid of challenging assumptions. Unafraid of challenges. Unafraid of success.

Intelligent We are curious,passionateand self-aware. We are agile,adaptableand seek diverse experience, knowledge, and skills to make informed, data driven decisions. Weanticipatethe needs of others, and we adapt quickly to challenges and find solutions. We rely on our collective experiences to diligently develop, strategicallyplanand efficiently execute our vision.

Unified We collaborate as we strive for excellence. We rely on each other, and we have each others backs. We encourage constructive feedback to continually improve. We support each other; we laugh together. We celebrate each others successes and band together in times of hardship. We foster and appreciate genuine relationships.

Our values underpinthe employeeexperience at LB Pharmaceuticals. They are the character and personality of the companydemonstratedthrough how we communicate, support one another, spend our time, make decisions, and celebrate collectively.