Senior SAS Statistical Programmer & CRO Lead

TG Therapeutics, Inc.; United States; On-site; USD 80,000 - 120,000; Full time

Job summary

A leading biotechnology company in the United States is seeking a Statistical Analyst to join their team. The role involves developing and validating statistical programs using SAS for clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams. Ideal candidates should have at least 5 years of experience in statistical programming within the pharmaceutical field and possess a Master's degree in a related area.

Qualifications

• 5+ years of statistical programming experience in the pharmaceutical or biotechnology industry.
• Good understanding of CDISC standards (SDTM, ADaM).
• Experience working with CROs and overseeing deliverables.

Responsibilities

• Develop and maintain SAS programs for clinical trial data analysis.
• Perform quality control checks and program validations.
• Act as a leading analyst in cross-functional teams.

Skills

SAS programming

Statistical analysis

Collaboration skills

Problem-solving

Education

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

Tools

SAS

R

Job description

A leading biotechnology company in the United States is seeking a Statistical Analyst to join their team. The role involves developing and validating statistical programs using SAS for clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams. Ideal candidates should have at least 5 years of experience in statistical programming within the pharmaceutical field and possess a Master's degree in a related area.