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Lead Statistical Programmer Jobs (NOW HIRING)

IQVIA

Principal Statistical Programmer

Durham, NC

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Lead and perform development and validation of: * SDTM datasets * ADaM datasets * Tables, Listings ...

Syneoshealth

Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables. Reviews project documentation such as ...

IQVIA

Principal Statistical Programmer

Durham, NC

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Lead and perform development and validation of: * SDTM datasets * ADaM datasets * Tables, Listings ...

IQVIA, Inc.

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for mid-July Position Summary We are seeking ... Lead and perform development and validation of: * SDTM datasets * ADaM datasets * Tables, Listings ...

Rho

Senior Statistical Programmer

Durham, NC · On-site

As a Senior Statistical Programmer, you'll have the opportunity to design and write program ... Lead and participate in the development and validation of high quality CDISC datasets based on the ...

Rho Inc

Senior Statistical Programmer

As a Senior Statistical Programmer, you'll have the opportunity to design and write program ... Lead and participate in the development and validation of high quality CDISC datasets based on the ...

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Lead Statistical Programmer information

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How much do lead statistical programmer jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for lead statistical programmer in the United States is $54.96, according to ZipRecruiter salary data. Most workers in this role earn between $43.27 and $68.75 per hour, depending on experience, location, and employer.

What is the difference between Lead Statistical Programmer vs Statistical Programmer?

AspectLead Statistical ProgrammerStatistical Programmer
CredentialsTypically requires a Bachelor's or Master’s in Biostatistics, Statistics, or related field; experience in clinical trialsSame educational background; entry to mid-level experience
Work EnvironmentLeads project teams, manages timelines, and oversees statistical analysisPerforms statistical programming tasks under supervision
Industry UsageUsed across pharmaceutical, biotech, and CROs for leadership rolesCommonly employed in similar settings for technical execution

The main difference between a Lead Statistical Programmer and a Statistical Programmer lies in leadership responsibilities, project management, and oversight. The Lead typically manages teams and ensures project delivery, while the Statistical Programmer focuses on executing statistical analyses under guidance.

What does a Lead Statistical Programmer do?

A Lead Statistical Programmer oversees and manages the programming aspects of clinical trial data analysis. They are responsible for developing, validating, and maintaining statistical programs used to analyze clinical data, typically using software like SAS. In addition to technical programming, they coordinate with statisticians, data managers, and project teams to ensure data integrity and compliance with regulatory standards. Lead Statistical Programmers often mentor junior programmers and play a key role in project planning and timeline management.

What are some common challenges faced by a Lead Statistical Programmer, and how can they be managed?

Lead Statistical Programmers often encounter challenges such as balancing multiple project timelines, ensuring compliance with regulatory standards, and coordinating effectively with cross-functional teams like biostatistics and clinical operations. Managing these challenges requires strong organizational and communication skills, as well as a proactive approach to problem-solving and stakeholder engagement. Regularly updating programming knowledge and fostering collaboration within the team can also help streamline workflows and maintain high-quality deliverables.

What are the key skills and qualifications needed to thrive as a Lead Statistical Programmer, and why are they important?

To thrive as a Lead Statistical Programmer, you need expertise in statistical programming languages like SAS or R, a solid understanding of clinical trial data, and a relevant degree in statistics, mathematics, or a related field. Familiarity with CDISC standards (SDTM, ADaM), regulatory submission processes, and version control systems are essential technical requirements. Strong leadership, communication, and problem-solving skills help in managing teams and collaborating across departments. These skills ensure accurate, compliant data analysis and efficient project delivery in a highly regulated environment.
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Lead Statistical Programmer jobs near you
Infographic showing various Lead Statistical Programmer job openings in the United States as of June 2026, with employment types broken down into 97% Full Time, and 3% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $114,323 per year, or $55 per hour.
Sr. Statistical Programmer

Sr. Statistical Programmer

Katalyst HealthCares & Life Sciences

Omaha, NE • On-site

Other

Posted 12 days ago

Job description

Statistical Programmer

Responsibilities:

  • Ensures that statistical deliverables (tables, figures, listings) and study datasets (SDTM, ADaM) are programmed and validated in accordance with standards requirements of regulatory agencies.
  • Assesses study datasets and resolves deviations from CDISC using Pinnacle21 or other quality tools
  • Maintains a basic understanding of relevant industry trends in standards implementation, clinical statistical programming, and ophthalmology
  • Provides technical consultation and collaborates with internal and external stakeholders to facilitate understanding of statistical programming services. Supports collaboration with Data Management to facilitate SDTM development
  • Develops programming efficiencies (eg, local macros) to ensure efficient programming work
  • Supports the development and rollout of new innovations, standards, processes, and programming efficiencies within Biostatistics
  • Develops specification documents for datasets, and all other supporting documents (eg, define.xml, annotated CRFs, reviewer's guides)
  • Develops programming efficiencies (eg, global macros) to ensure consistent and efficient work across studies
  • Leads and manages statistical programming priorities and task assignments for clinical studies and submissions
  • Tracks and escalates concerns related to changes in scope of services
  • Mentors junior statistical programmers

Requirements:

  • Bachelor's or master's degree or international equivalent in Biostatistics, Statistics, or programming-related field
  • 5 or more years of experience supporting clinical trials for regulatory submissions with sufficient experience as a study or program lead, preferred
  • A high level of SAS programming skills including SQL and macro development
  • Good knowledge and application of CDISC standards for SDTM and ADaM
  • Experience with Pinnacle21 and writing reviewer's guides is a plus
  • Basic understanding of standard statistical methodologies is expected
  • Experience with ophthalmology is preferred
  • Good understanding of statistical programming topics in medical product development
  • Excellent technical and programming logic skills
  • A successful history of cross-functional collaboration
  • Sound knowledge of all relevant regulations and guidelines
  • Excellent verbal and written communication skills
  • Good planning and organizational skills with the ability to adapt and adjust to changing priorities
  • Ability to be productive and handle multiple tasks to meet deadlines in a dynamic, fast-paced environment
  • A strong interest in developing expertise in ophthalmology
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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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