Lead Statistical Programmer – Clinical Trials

ClinChoice; Northern (KY); Hybrid; USD 110,000 - 140,000; Full time

Job summary

ClinChoice is seeking a Senior Statistical Programmer to join our in-house team in the United States. This permanent role supports projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health sectors.

You will lead statistical activities with hands-on expertise and independently manage projects while collaborating with cross-functional teams. You will program and validate SDTM/ADaM outputs, contribute to CDISC submissions, and oversee

Qualifications

• Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
• BS with more than 5 years or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
• Strong SAS and SAS Macro language skills.
• R programming skills in clinical trials.
• Familiarity with the drug development process.
• Strong oral and written communication skills.

Responsibilities

• Lead statistical programming activities for clinical trials.
• Program and validate derived datasets, tables, figures, listings.
• Oversee programming deliverables from CROs.
• Collaborate with cross-functional teams and external vendors.
• Ensure programming deliverables are on time and of high quality.

Skills

SAS programming

R programming

SAS Macro language

Data integration

Communication skills

Education

Bachelor's or Master’s degree in a related field

Tools

SAS

R

Job description

ClinChoice is seeking a Senior Statistical Programmer to join our in-house team in the United States. This permanent role supports projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health sectors.

You will lead statistical activities with hands-on expertise and independently manage projects while collaborating with cross-functional teams. You will program and validate SDTM/ADaM outputs, contribute to CDISC submissions, and oversee