Senior Statistician

Abbott

3-8 years

$90,000.00 – $180,000.00

United States

10 Jan. 6, 2026

Job Description

Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 Statistician – Medical & Clinical Affairs

Location: Alameda, California, United States
Category: Medical & Clinical Affairs
Experience Required: 3–8 years
Employment Type: Full-time | Onsite

Company Overview

Abbott is a globally recognized healthcare leader dedicated to helping people live healthier lives at every stage. With operations in over 160 countries and a workforce of more than 114,000 professionals, Abbott delivers innovative solutions across diagnostics, medical devices, nutrition, and branded generic pharmaceuticals. The company is consistently ranked among the world’s most admired and best places to work.

Role Overview

Abbott is seeking a highly skilled Senior Statistician to join its Tech Operations division in Alameda, California. This role plays a critical part in clinical research and product development by providing advanced statistical expertise across protocol design, data analysis, regulatory submissions, and scientific reporting.

The Senior Statistician will work closely with cross-functional teams including clinical research, regulatory affairs, and project leadership, contributing to high-impact clinical programs while ensuring compliance with global regulatory standards.

Key Responsibilities

Protocol Design, Randomization & Database Activities

Collaborate with cross-functional project teams to determine appropriate study designs and statistical methodologies.
Perform comprehensive protocol reviews to ensure scientific and regulatory rigor.
Develop randomization schedules and conduct sample size and power calculations.
Ensure accuracy and integrity of clinical data used for statistical analysis.

Statistical Analysis & Methodology

Implement statistical analysis plans in alignment with approved protocols.
Ensure accuracy, efficiency, and documentation of statistical programming outputs.
Evaluate and validate alternative analysis strategies when protocol deviations or changes occur.
Demonstrate advanced knowledge of statistical concepts and methodologies applicable to clinical research.

Scientific Reports & Publications

Author and review Statistical Methods sections of clinical study reports.
Ensure accuracy and consistency of statistical tables, listings, and report narratives.
Identify and correct flaws in data interpretation, presentation inconsistencies, and inference errors.
Provide strategic input into report development and publication planning.

Consultation & Cross-Functional Collaboration

Provide statistical consultation to internal stakeholders and project teams.
Respond accurately and efficiently to routine and complex statistical inquiries.
Present statistical concepts clearly to management, regulatory authorities, and scientific audiences.
Support clinical program strategy development with data-driven insights.
Build and maintain strong internal and external stakeholder relationships.

Training, Mentorship & Leadership

Mentor junior statisticians and non-statistical team members on statistical methodology.
Lead teams of statisticians and programmers on assigned clinical trials.
Deliver formal training sessions for statisticians and cross-functional partners.
Act as a project leader on key initiatives within the department.

Regulatory & Project Coordination

Ensure statistical contributions meet regulatory requirements for submissions and development decisions.
Coordinate statistical activities across multiple projects and therapeutic areas.
Collaborate closely with Regulatory Affairs to support filings and agency interactions.
Communicate project status, risks, and resource needs to senior management.

Required Qualifications

Bachelor’s degree in Statistics or Mathematics (required).
Master’s degree with a minimum of 5 years of relevant experience or
PhD with a minimum of 3 years of relevant industry or clinical research experience (preferred).
Strong experience in clinical trial statistics, regulated environments, or healthcare product development.
Proven ability to manage competing priorities and deliver high-quality outputs within timelines.
Excellent written and verbal communication skills with the ability to explain statistical concepts to non-statisticians.

Compensation

The base salary range for this position is USD 90,000 – 180,000, depending on experience, qualifications, and geographic location. Compensation may vary based on business and market factors.

Why Join Abbott

Work on impactful clinical and scientific initiatives with a global healthcare leader.
Access long-term career growth opportunities in a multinational environment.
Competitive compensation and comprehensive benefits including healthcare, retirement, and education assistance programs.
Inclusive and diverse workplace recognized for excellence, innovation, and employee well-being.

Industry Segment

Medical Devices | Clinical Research | Biostatistics

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Senior Statistician

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