Connexion-posted 2 months ago
$100 - $115/Yr
Principal
Remote • Boston, MA
11-50 employees

Connexion's mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve. Title: Principal Statistical Programmer (Contract) Hiring Organization: Connexion Systems & Engineering Compensation, Benefits, and Employment Type Duration: 6+ month contract (W2 ONLY) Pay rate: $100-$115/hr Job Location: 100% remote, EST/CST time zone Schedule: M-F, standard business hours, EST Job#: bh18160 Description: Our client, a leading global biopharmaceutical company, is seeking an experienced Principal Statistical Programmer to support key clinical development programs. The ideal consultant will be highly proficient in SAS programming, with a strong background in CDISC standards, NDA submissions, and end-to-end clinical data analysis. This is an excellent opportunity for an experienced statistical programmer to contribute to high-impact regulatory projects within a fast-paced and collaborative environment. Interested candidates should apply as soon as possible. This role is expected to fill quickly. Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly. You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line. If you are active in a job search but this job is not for you, please reach out to [email protected]. We would be glad to help you find the perfect job!

  • Lead statistical programming activities for clinical studies and integrated submissions.
  • Develop, validate, and maintain SAS programs for ADaM datasets, tables, listings, and figures (TFLs).
  • Create and QC CDISC-compliant SDTM and ADaM datasets, Define.xml, and electronic submission deliverables.
  • Collaborate closely with Biostatistics, Data Management, and Clinical Operations teams to ensure data accuracy and consistency.
  • Perform ad hoc analyses and data integration across studies.
  • Review programming specifications and study documentation.
  • Oversee and QC CRO deliverables.
  • Advanced SAS programming expertise.
  • Minimum 5 years of experience in pharmaceutical, biotech, or CRO clinical programming.
  • Proven experience with SDTM and ADaM programming.
  • Strong understanding of CDISC standards and NDA submission processes.
  • Hands-on TFL generation and QC experience.
  • Bachelor's degree or higher in Statistics, Mathematics, Computer Science, or related discipline.
  • Familiarity with R or other statistical programming languages (a plus).
  • Strong communication skills and the ability to work effectively within cross-functional teams.
  • Proven ability to manage multiple projects and shifting priorities in a fast-paced environment.
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