Senior Statistical Programmer — Clinical Trials

Cytel; Hartford (CT); On-site; USD 150,000 - 190,000; Full time

Job summary

Cytel is seeking a Principal Statistical Programmer to work embedded with a pharma client, delivering high-quality programming for clinical studies. You will lead the development of SDTM/ADaM datasets, define.xmls, and reviewer’s guides while driving regulatory submissions readiness.

The role emphasizes independent work, leadership, and the ability to mentor others, with ongoing exposure to evolving technologies and collaboration across CROs and vendors.

Qualifications

• Must have 9+ years of experience as a Statistical Programmer in Biotech/Pharma clinical development or equivalent.
• Exceptional SAS/R programming skills and experience in clinical development environments.
• Extensive experience with CDISC standards (SDTM, ADaM, Define.xml) and regulatory submissions.

Responsibilities

• Generate SDTM/ADaM datasets, define.xml, and reviewer’s guides for multiple studies.
• Lead SAS/R programming to produce tables, listings, and graphs of high quality.
• Support regulatory submissions and create documentation for programming standards.

Skills

Leadership

Communication

Independent work

Project delivery

Education

Bachelor’s degree in computer science, data science, mathematics, or statistics

Tools

SAS

R

Job description

Cytel is seeking a Principal Statistical Programmer to work embedded with a pharma client, delivering high-quality programming for clinical studies. You will lead the development of SDTM/ADaM datasets, define.xmls, and reviewer’s guides while driving regulatory submissions readiness.

The role emphasizes independent work, leadership, and the ability to mentor others, with ongoing exposure to evolving technologies and collaboration across CROs and vendors.