Senior Statistical Programmer – SAS, CDISC, Remote

Kapres Technology; Málaga; Remote; EUR 65,000 - 95,000; Full time

Job summary

Cytel Inc. is seeking a Senior Statistical Programmer to leverage advanced SAS programming and CDISC SDTM/ADaM expertise to support or lead Phase I–IV clinical trials.

This role can be performed fully remotely, working with a global pharmaceutical client. You will design, implement and validate datasets, tables, listings and figures, perform data manipulation and analysis, and contribute to submission documents while collaborating with cross-functional teams.

Qualifications

• Bachelor's degree in Statistics, Computer Science, Mathematics, or equivalent.
• At least 8 years of SAS programming in the Pharmaceutical & Biotech industry with a bachelor's, or 6+ years with a master's.
• Study lead experience preferred with ability to juggle multiple projects.
• Strong SAS data manipulation, analysis and reporting skills.
• Solid CDISC SDTM/ADaM experience.
• QC/validation skills and ad-hoc reporting proficiency.
• Proficiency in Efficacy analysis and drug development lifecycle familiarity.
• Submissions experience with define.xml and related documents.
• Experience supporting immunology, respiratory, or oncology studies is a plus.
• Excellent analytical and troubleshooting abilities; capable of delivering high-quality output on tight timelines.
• Ability to work effectively in a globally dispersed team with cross-cultural partners.

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy).
• Generate and validate SDTM and ADaM datasets/analysis files and TLFs.
• Production and QC/validation programming.
• Create and review submission documents and eCRTs.
• Communicate with internal cross-functional teams and clients on specifications and status.
• Lead projects when called upon and collaborate effectively with a globally dispersed team.

Skills

SAS programming

Data analysis

Efficacy analysis

CDISC SDTM/ADaM

Ad-hoc reporting

Study lead experience

QC/validation skills

Cross-functional communication

Troubleshooting

Leadership duties

Education

Bachelor's degree in Statistics/Computer Science/Mathematics

Master's degree (preferred) with more experience

Tools

SAS software

define.xml (submission documents)

Job description

Cytel Inc. is seeking a Senior Statistical Programmer to leverage advanced SAS programming and CDISC SDTM/ADaM expertise to support or lead Phase I–IV clinical trials.

This role can be performed fully remotely, working with a global pharmaceutical client. You will design, implement and validate datasets, tables, listings and figures, perform data manipulation and analysis, and contribute to submission documents while collaborating with cross-functional teams.