Senior SAS Programmer - Remote (CDISC SDTM/ADaM)

Miscota

Málaga

Remote

EUR 65,000 - 90,000

Full time

2 days ago

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Job summary

Senior Statistical Programmer at Cytel Inc. is embedded with a pharmaceutical client, focusing on SAS programming and CDISC SDTM/ADaM usage for Phase I-IV trials. This role can be performed fully remotely, with global collaboration across teams.

You will lead data manipulation, analysis, and reporting of safety and efficacy data, generate TLFs, and contribute to submission documents while delivering high-quality outputs within tight timelines.

Qualifications

Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
8 years SAS programming with clinical trial data; 6+ years with master's degree.
Study lead experience preferred.
Strong SAS data manipulation, analysis and reporting skills.
CDISC SDTM/ADaM standards experience.
Strong QC/validation skills.
Good ad-hoc reporting skills.
Proficiency in efficacy analysis.
Familiarity with drug development lifecycle and trial data.
Submissions experience with define.xml and submission documents.
Experience with immunology, respiratory or oncology studies a plus.
Excellent analytical & troubleshooting skills.
Ability to deliver quality outputs under tight timelines.
Ability to work in a globally dispersed team.

Responsibilities

Perform data manipulation, analysis and reporting of clinical trial data (ISS/ISE) using SAS.
Generate and validate SDTM and ADaM datasets/analysis files and TLFs.
Production and QC/validation programming.
Generate complex ad-hoc reports from raw data.
Apply strong understanding of efficacy analysis.
Create and review submission documents and eCRTs.
Communicate with cross-functional teams and clients on specs and status.
Lead duties when called upon.
Be a team player and adapt to changing priorities.