Statistical Programmer

Apr; United States; Remote; USD 85,000 - 130,000; Full time

Job summary

A leading company in health economics and outcomes research is seeking a Consultant Statistical Programmer for a remote, 12-month renewable contract. The successful candidate will support RWE and HEOR initiatives, collaborating with biostatisticians and handling statistical programming tasks using SAS and R. Key responsibilities include developing high-quality statistical outputs and maintaining compliance with industry standards.

Qualifications

• Minimum 4 years of experience in clinical research.
• Hands-on experience with CDISC SDTM and ADaM datasets.
• Proficiency in SAS and R programming is required.

Responsibilities

• Collaborate with biostatisticians to provide statistical programming support.
• Develop and maintain SAS/R programs for HEOR and RWE studies.
• Ensure programming activities comply with industry standards.

Skills

Analytical Skills

Problem Solving

Statistical Techniques

Education

Master’s degree in Statistics, Biostatistics, Mathematics, or Computer Science

Tools

SAS

R

Job description

To Apply for this Job Click Here

Remote, 12-month renewable contract

Position Summary:

We are seeking a highly skilled and detail-oriented Consultant Statistical Programmer to support Real-World Evidence (RWE) and Health Economics and Outcomes Research (HEOR) initiatives. The successful candidate will work closely with the RWE/HEOR biostatistician and will be responsible for developing, executing, and validating statistical programs using SAS and/or R to support analyses and deliverables for RWE, HEOR, and Market Access activities.

Responsibilities:

• Collaborate with HEOR and RWE biostatisticians to provide statistical programming support across various projects.
• Develop, validate, and maintain SAS and/or R programs to support statistical analyses and reporting activities for HEOR, RWE, and Market Access studies.
• Generate high-quality tables, listings, and figures based on clinical trial data and other relevant data sources.
• Perform statistical modeling and analyses as required.
• Utilize SDTM and ADaM datasets to derive analysis datasets.
• Serve as the primary programmer on assigned projects, ensuring that programming deliverables are accurate and consistent.
• Perform quality control (QC) on statistical programs and outputs as needed.
• Ensure all programming activities comply with industry standards, study protocols, and statistical analysis plans (SAPs).
• Provide input on statistical methodologies and contribute to project deliverables.
• Maintain comprehensive documentation and audit trails for all programming activities.
• Perform rigorous data quality checks to ensure accuracy, completeness, and consistency.

Education & Experience Requirements:

• Master’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related technical discipline with emphasis on statistics.
• Minimum of 4 years of experience in clinical research, preferably within the pharmaceutical or CRO industry, with exposure to Phase I–IV trials.
• Hands-on experience with CDISC SDTM and ADaM datasets.
• Proficiency in SAS and R programming is required

Additional Skills & Experience:

• Strong analytical and problem-solving skills, with the ability to manage complex studies and meet deadlines.
• Experience with statistical techniques, including longitudinal data analysis, survival analysis, and statistical modeling/simulation.
• Familiarity with observational studies, causal inference, patient-reported outcomes (PROs), and health technology assessment (HTA)
• Experience with indirect treatment comparisons (ITCs), such as matching-adjusted indirect comparison (MAIC), is a plus.
• Prior experience in a similar role within the pharmaceutical industry, preferably with a focus on small molecule pharmaceuticals.

To Apply for this Job Click Here