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Lead Statistical Programmer Jobs (NOW HIRING)

IQVIA

Senior Statistical Programmer

Durham, NC · On-site +1

$139K - $165K/yr

Serve as the programming lead across multiple clinical studies, overseeing the development and delivery of high-quality statistical programming outputs. Design and implement clinical data standards ...

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Lead Statistical Programmer information

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$10

$54

$83

How much do lead statistical programmer jobs pay per hour?

As of Jul 23, 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 July 2026, with employment types broken down into 88% Full Time, 9% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $114,323 per year, or $55 per hour.
Sr. Statistical Programmer

Sr. Statistical Programmer

Kodiak Sciences Inc.

Palo Alto, CA

Full-time

Posted 28 days ago

Job description

Kodiak Sciences Inc. is a rapidly growing, clinical-stage biopharmaceutical company dedicated to transforming ophthalmology through innovative therapeutics. Our proprietary Antibody Biopolymer Conjugate Drug (ABCD) platform integrates protein engineering, polymer chemistry, small molecule drug discovery, and advanced drug delivery technologies to address prevalent and debilitating retinal diseases with the goal of improving patient outcomes worldwide. In this fast-growing and fast-paced organization, your expertise is needed to provide support for clinical and statistical programming activities related to multiple clinical studies.

Key Responsibilities

  • Assist in the review of key study-related documents produced by other functions, e.g. Statistical Analysis Plan, Case Report Forms, Data Management Plan, Database Specifications, EDC Data Structures, DMC plans and other clinical documents
  • Write, test and validate SAS programs to produce analysis datasets, TLFs, to be included in reports for submission to regulatory agencies, publications and other communications as needed
  • May serve as a technical lead and project manager for multiple studies managing all aspects of study deliverables related to statistical and clinical programming as needed
  • Work with internal stakeholders to gather requirements and write specifications
  • Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Monitors to address programming related study deliverables
  • Write macros for reusability
  • Review and verify vendor deliverables for quality and accuracy
  • Contribute to the development review of Statistical Programming policies, standard operating procedures and other controlled documents
  • Interface with outsourcing partners and vendors

Education & Experience

  • B.S. preferably in Mathematics, statistics, computer sciences or other related field
  • 5+ years of clinical trials experience in pharmaceutical or biopharmaceutical setting or equivalent

Additional Skills

  • Thorough knowledge of the drug development and regulatory submission cycle
  • Excellent project management skills
  • Excellent communication skills
  • Able to work in a fast pace and agile environment
  • In-depth and current knowledge of regulatory requirements and guidance
  • Excellent SAS and CDISC skills
  • Proficiency in MS Word, Excel, PowerPoint, and Project