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Principal Statistical Programmer FSP

Cytel
Remote, IND
Full-time
Lead · 7+ years experience
Remote
Discovered 1 weeks ago
CommunicationPythonJava

Full Job Posting

Qualifications

  • Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
  • At a minimum bachelor’s degree in computer science, data science, mathematics, or statistics major preferred
  • 7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies
  • Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment
  • Extensive applied experience of CDISC standards (SDTM, ADaM, and Define.xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation
  • Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities
  • Must be able to work independently
  • Outstanding communication skills (written and verbal) and strong leadership skills
  • Preferred Qualifications (nice to have)
  • Prior work experience with pharmacokinetic data and the neuroscience field,
  • proficiency in languages or tools other than SAS (e.g., R, Python, and Java, Shiny, Markdown, Unix/Linux and git)

Responsibilities

  • As a Principal Statistical Programmer, your responsibilities will include:
  • Generate SDTM, ADaM specifications, datasets, reviewer’s guide and define.xml files for multiple studies
  • Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
  • Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs’ needs
  • Participate in overseeing CRO’s statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
  • Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
  • Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
  • Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
  • Participate in the development of CRFs, edit check specifications, and data validation plans
  • Provide review and/or author data transfer specifications for external vendor data
  • Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
  • Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices

Preferred Qualifications

  • At a minimum bachelor’s degree in computer science, data science, mathematics, or statistics major preferred
  • Preferred Qualifications (nice to have)

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