Jefe/A De Proyecto De Transformación Principal Con Catalán (M/F/D)

T-Systems Iberia

Granada

Remote

EUR 99,000 - 152,000

Full time

6 days ago
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Benefits offered by this job

Remote work

Job summary

Cytel Inc. seeks a Senior/Principal Statistical Programmer to support or lead Phase I‑IV clinical trials, leveraging SAS programming and CDISC SDTM/ADaM standards.

This sponsor-dedicated role can be performed fully remote and places you at the heart of a client-driven development program. You will manipulate and analyze data, create submission-ready datasets and reports, lead study activities, and collaborate with globally dispersed teams to deliver timely, high-quality outputs within project

Qualifications

  • Bachelor’s degree in Statistics, Computer Science, Mathematics or related field.
  • 8+ years of SAS programming in pharmaceutical/biotech; 6 years with a master’s.
  • Experience leading studies and juggling multiple projects.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid SDTM/ADaM implementation experience.
  • QC/validation and ad-hoc reporting capabilities.
  • Proficiency in efficacy analysis and drug development lifecycle.

Responsibilities

  • Perform data manipulation, analysis and reporting of clinical trial data, safety and efficacy.
  • Generate and validate SDTM and ADaM datasets.
  • 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 internal teams and client for project specifications.
  • Perform lead duties when called upon.
  • Serve as team player and meet deadlines.
  • Be adaptable and flexible with changing priorities.

Skills

SAS data manipulation
Efficacy analysis
ADaM/SDTM data analysis
Ad-hoc reporting
QC/validation
Team collaboration

Education

Bachelor's degree in Statistics, Computer Science, Mathematics or related

Tools

SAS
R
CDISC SDTM/ADaM
Define.xml

Job description

Senior/Principal Statistical Programmer SAS + R (Remote)

Sponsor-dedicated

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel. You will be at the heart of our client's innovation. This is an exciting time to be part of this new program.

Position Overview

Senior Statistical Programmer skilled in SAS programming and CDISC standards (SDTM & ADaM) to support or lead Phase I‑IV clinical trials. This role can be performed fully remote.

Our values

  • We believe in applying scientific rigor to reveal data promise.
  • We nurture intellectual curiosity and encourage new challenges.
  • We collaborate and invite diversity of perspectives.
  • We prize innovation and intelligent solutions.

How you will contribute

  • Perform data manipulation, analysis and reporting of clinical trial data, safety and efficacy.
  • Generate and validate SDTM and ADaM datasets.
  • 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 internal teams and client for project specifications.
  • Perform lead duties when called upon.
  • Serve as team player and meet deadlines.
  • Be adaptable and flexible with changing priorities.

Requirements

  • Bachelor's degree in Statistics, Computer Science, Mathematics or related.
  • At least 8 years of SAS programming in pharmaceutical or biotech; 6 years with a master’s.
  • Study lead experience, preferably juggling multiple projects.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid experience implementing SDTM / ADaM standards.
  • Strong QC / validation skills.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle.
  • Define.xml and other submission document experience.
  • Experience in immunology, respiratory or oncology studies a plus.
  • Excellent analytical and troubleshooting skills.
  • Ability to provide quality output and deliverables within timelines.
  • Collaborate in a globally dispersed team.

LI-KO1

Cytel Inc. is an Equal Employment /affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression or any other protected characteristic.

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