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Senior Statistician – Medical Device Clinical Research

Abbott
Abbott
5-10 years
Not Disclosed
Alameda, California, United States
2 May 8, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, 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

Senior Statistician – Medical Device Clinical Research Job in California, USA

Company: Abbott Laboratories
Job Title: Senior Statistician
Location: Alameda, California, USA
Department: Medical and Clinical Affairs – Tech Ops Division
Job Type: Full-Time
Industry: Medical Devices / Clinical Research / Biostatistics


About Abbott

Abbott is a global healthcare leader focused on improving lives through innovative diagnostics, medical devices, nutrition products, and pharmaceutical solutions. With operations in over 160 countries and a workforce of more than 115,000 professionals worldwide, Abbott continues to drive advancements in healthcare technology and clinical research.

Abbott’s Medical Devices division develops advanced healthcare technologies that improve patient outcomes in cardiology, diabetes care, chronic pain management, and other critical healthcare areas.


Job Overview

Abbott is seeking an experienced Senior Statistician to join its Tech Ops Medical Devices division in Alameda, California. This role involves leading statistical activities for clinical studies, supporting protocol development, designing statistical methodologies, performing advanced analyses, and contributing to regulatory submissions and scientific publications.

The selected candidate will collaborate with clinical teams, regulatory affairs, programmers, and research scientists to ensure accurate statistical analysis, high-quality reporting, and compliance with regulatory standards.

This opportunity is ideal for experienced biostatistics and clinical research professionals with expertise in statistical methodologies, medical device clinical studies, regulatory support, and scientific reporting.


Experience Required

Experience Level

  • Senior-Level Statistician / Biostatistics Professional
  • Freshers are not eligible

Required Experience

Candidates should meet one of the following:

  • MS/MA with 5+ years of related work experience
    or
  • PhD with 3+ years of related work experience

Preferred Experience

  • Clinical Research Statistics
  • Medical Device Clinical Trials
  • Statistical Programming
  • Regulatory Submission Support
  • Clinical Data Analysis
  • Protocol Design & Statistical Methodology

Educational Qualification

Required Qualification

  • Bachelor’s Degree in:
    • Statistics
    • Mathematics
    • Biostatistics
    • Related analytical discipline

Preferred Qualification

  • MS / MA in Statistics or related field
  • PhD in Statistics, Biostatistics, Mathematics, or related discipline