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Senior Statistical Programmer Fsp

8+ years
Not Disclosed
10 Feb. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Statistical Programmer FSP
Location: Remote India
Job Type: Full-time
Posted: Feb. 13, 2025
Job ID: 330

Position Overview:

As a Senior Statistical Programmer, you'll be embedded within one of Cytel’s pharmaceutical clients, playing a key role in supporting Phase I-IV clinical trials. Using your advanced SAS programming skills and expertise in CDISC standards (SDTM & ADaM), you’ll help drive innovations in patient treatment. This role offers the flexibility of fully remote work.

Responsibilities:

  • Perform data manipulation, analysis, and reporting of clinical trial data (safety and efficacy) using SAS programming.

  • Generate and validate SDTM and ADaM datasets, analysis files, tables, listings, and figures (TLFs).

  • Apply strong understanding and experience in efficacy analysis.

  • Create and review submission documents such as eCRTs.

  • Communicate with internal teams and clients regarding project specifications, statuses, issues, or inquiries.

  • Lead projects and collaborate with teams to meet deadlines.

Qualifications:

  • Experience: At least 8 years of SAS programming in clinical trial data (Pharmaceutical & Biotech industry). A minimum of 6 years with a master’s degree.

  • Education: Bachelor's degree in Statistics, Computer Science, Mathematics, or similar field.

  • Skills:

    • Expertise in SAS data manipulation, analysis, and reporting.

    • Solid experience in CDISC SDTM/ADaM standards.

    • Proficiency in Efficacy analysis and submission experience (define.xml).

  • Other: Experience supporting immunology, respiratory, or oncology studies is a plus.

Additional Information:

  • Location: Remote positions available in multiple countries (UK, Germany, France, Spain).

  • Cytel’s Values: We are dedicated to intellectual curiosity, collaboration, and innovation in clinical development.

Apply now and be part of Cytel's mission to advance the state of clinical development!

Apply Now