Senior Statistical Programmer, Clinical Trials Lead

Syneos Health; Indiana (PA); On-site; USD 110,000 - 150,000; Full time

Job summary

Syneos Health in the United States is seeking a Sr. Statistical Programmer clinpharm to develop and validate SAS programs that generate tables, listings, and figures aligned with SAPs and specifications.

The role leads programming activities, mentors junior staff, and collaborates with biostatisticians and project teams to ensure timely delivery and regulatory compliance across multiple studies.

Qualifications

• Undergraduate degree or equivalent combination of education and programming experience.
• Extensive SAS programming experience in a clinical trial environment.
• Excellent written and verbal communication skills.
• Ability to read, write, speak and understand English.

Responsibilities

• Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the SAP and programming specs.
• Ensure outputs meet quality standards and project requirements; perform validation programming and coordinate with team to resolve discrepancies.
• Maintain organized project documentation and ensure inspection readiness.
• Manage scheduling/time constraints across multiple projects; develop specifications for datasets and outputs; anticipate programming issues and define variables clearly.

Skills

SAS programming

Statistical analysis

Communication skills

English proficiency

Education

Bachelor's degree in a scientific or statistical field

Job description

Syneos Health in the United States is seeking a Sr. Statistical Programmer clinpharm to develop and validate SAS programs that generate tables, listings, and figures aligned with SAPs and specifications.

The role leads programming activities, mentors junior staff, and collaborates with biostatisticians and project teams to ensure timely delivery and regulatory compliance across multiple studies.