Senior Statistical Programmer (Remote) - SDTM/ADaM Expert

Cytel; Columbus (OH); On-site; USD 110,000 - 170,000; Full time

Job summary

Cytel is seeking a Senior Statistical Programmer to support one or more Phase I-IV clinical trials, leveraging advanced SAS skills and CDISC SDTM/ADaM expertise.

The role can be performed fully remotely and involves data manipulation, analysis, and reporting, including creating TLFs and submission documents. Strong Efficacy analysis experience and excellent collaboration with global teams are essential.

Qualifications

• Bachelor’s degree in Statistics, Computer Science, Mathematics, or related field.
• At least 8 years of SAS programming in the Pharmaceutical/Biotech industry with a bachelor’s; 6+ years with a master’s.
• Experience leading studies and juggling multiple projects is preferred.
• Strong SAS data manipulation, analysis and reporting skills.
• Solid experience implementing CDISC SDTM/ADaM standards.
• Proficiency in efficacy analysis and submission document preparation.
• Ability to work with global teams and meet timelines.

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy) using SAS.
• Generate and validate SDTM/ADaM datasets and TLFs.
• Produce and QC/validate programming outputs and reports.
• Create complex ad-hoc reports from raw data.
• Review submission documents and eCRTs.
• Coordinate with cross-functional teams and client on specifications and status.
• Lead duties when called upon and mentor junior staff.
• Adapt to changing priorities and work across a dispersed team.

Skills

SAS programming

CDISC SDTM/ADaM

Clinical trials

Data manipulation

Ad-hoc reporting

Education

Bachelors in Statistics/CS/Math

Master's degree preferred

Tools

SAS

Job description

Cytel is seeking a Senior Statistical Programmer to support one or more Phase I-IV clinical trials, leveraging advanced SAS skills and CDISC SDTM/ADaM expertise.

The role can be performed fully remotely and involves data manipulation, analysis, and reporting, including creating TLFs and submission documents. Strong Efficacy analysis experience and excellent collaboration with global teams are essential.