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Sr. Statistical Programmer - Fsp - Us West Coast Only

4+ years
USD 104,000 – USD 145,000 annually
10 Nov. 27, 2025
Job Description
Job Type: Full Time Remote 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

Senior Statistical Programmer – FSP (US West Coast Only)

Location: Remote, California, USA
Job ID: R-01330166
Job Type: Full-Time
Category: Clinical Research
Work Model: Fully Remote


About the Role

Thermo Fisher Scientific’s PPD® clinical research services support the development of innovative therapies across more than 100 countries. As part of this global CRO network, we are seeking a Senior Statistical Programmer (FSP Model) to lead complex data programming, analysis, and submission activities for clinical trials.

This role requires candidates residing on the US West Coast and legally authorized to work in the United States without sponsorship. A full background check and drug screening will be required.


Position Overview

The Senior Statistical Programmer will provide advanced SAS and statistical programming expertise, lead high-complexity data analysis projects, support CDISC deliverables, and ensure compliance with regulatory and industry standards. This is a client-dedicated role within our Functional Service Provider (FSP) model, offering exposure to large-scale clinical programs and global teams.


Key Responsibilities

Advanced Programming & Data Analysis

  • Develop, validate, and maintain complex statistical programs for clinical trial analysis.

  • Perform detailed quality control checks on SAS code, datasets, and outputs.

  • Lead and execute high-complexity data analysis and reporting projects.

CDISC & Regulatory Deliverables

  • Develop programs for electronic submission in CDISC SDTM and ADaM formats.

  • Review statistical analysis plans and programming specifications.

  • Ensure programming outputs meet regulatory, GCP, and industry standards.

Process Optimization & Documentation

  • Optimize programming workflows, tools, and methodologies for efficiency.

  • Maintain documentation, version control, and audit-ready records.

  • Troubleshoot and resolve programming and data issues promptly.

Team Leadership & Support

  • Provide technical guidance and mentorship to junior programmers.

  • Collaborate with cross-functional teams including biostatistics, data management, and clinical operations.


Experience Required

Minimum Requirements

  • 4+ years of statistical programming experience, ideally in clinical research or biopharmaceutical trials.

  • Strong proficiency in SAS; experience with R or Python is advantageous.

  • Experience developing SDTM and ADaM datasets following CDISC standards.

  • Bachelor’s degree in Statistics, Biostatistics, Computer Science, Data Science, or a related field.

Additional Requirements

  • Must be based on the US West Coast (California, Oregon, Washington, Nevada).

  • Must be legally authorized to work in the United States without sponsorship.

  • Must successfully pass a comprehensive background check and drug screen.


Skills & Competencies

  • Strong analytical and problem-solving skills.

  • Excellent attention to detail and accuracy in programming outputs.

  • Effective written and verbal communication skills.

  • Ability to lead, coach, and mentor junior team members.

  • Proficiency in standard office tools and statistical software environments.


Physical & Work Requirements

  • Ability to perform computer-based work for extended periods.

  • Occasional standing, walking, and light lifting (up to 25 lbs).

  • Ability to read, interpret, and type for long durations.


Compensation & Benefits

Estimated Salary Range (California):
USD 104,000 – USD 145,000 annually, based on role level and experience.

Additional benefits may include:

  • Annual performance-based bonus eligibility.

  • Comprehensive medical, dental, and vision plans.

  • Paid time off (minimum 120 hours), 10 annual paid holidays, and parental leave.

  • Employee assistance and family support programs.

  • Tuition reimbursement and commuter benefits.

  • 401(k) retirement savings plan and Employee Stock Purchase Plan (ESPP).