Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Statistician

5+ years
USD 86,700 – 173,300
10 Dec. 12, 2025
Job Description
Job Type: Full Time Remote 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 – Alameda, California

Category: Medical and Clinical Affairs
Company: Abbott Laboratories

Abbott is a global leader in healthcare innovation, delivering advanced technologies across diagnostics, medical devices, nutrition, and branded generic medicines. With more than 114,000 employees in over 160 countries, Abbott is committed to transforming health outcomes and advancing clinical science through evidence-driven solutions.


Position Overview

The Senior Statistician will join Abbott’s Tech Ops division in Alameda, California. This role provides advanced statistical leadership across protocol design, clinical research, data strategy, regulatory submissions, and scientific reporting. The position requires strong expertise in biostatistics, clinical data management, and cross-functional collaboration to support product development and regulatory compliance.


Key Responsibilities

Protocol Design and Statistical Planning

  • Collaborate with project teams to develop appropriate study designs and statistical methodologies.

  • Lead comprehensive protocol reviews and statistical input.

  • Develop randomization schedules, sample size calculations, and power assessments.

  • Ensure accuracy and completeness of datasets used for statistical analyses.

Statistical Analyses

  • Execute statistical analysis plans and oversee implementation of protocol methodology.

  • Ensure accuracy and timeliness of statistical deliverables for reports and decision-making.

  • Validate alternative analytical approaches when deviations from planned analyses are required.

  • Develop statistical programs that are accurate, efficient, and fully documented.

  • Demonstrate advanced knowledge of statistical concepts and methodologies.

Scientific Reporting and Publications

  • Prepare and ensure the accuracy of Statistical Methods and data tables.

  • Identify inconsistencies or errors in interpretation and reporting.

  • Provide timely input into report strategy and scientific documentation.

Consultation and Cross-Functional Leadership

  • Partner with internal teams to develop high-quality protocols, CRFs, and reports.

  • Provide timely responses to routine statistical queries and advanced scientific insights for complex questions.

  • Maintain strong client relationships and support strategies for engagement and expansion.

  • Present statistical concepts to scientific, regulatory, and management stakeholders.

  • Contribute to clinical program strategies and development pathways.

Training, Mentoring, and Leadership

  • Mentor less experienced statisticians and provide statistical training across teams.

  • Lead small teams of statisticians and programmers for assigned trials or projects.

  • Provide direction, motivation, and development opportunities for junior team members.

Project Coordination and Regulatory Support

  • Lead statistical activities for multiple projects, ensuring adherence to timelines and regulatory needs.

  • Collaborate with project leaders, regulatory affairs, and cross-functional teams.

  • Ensure statistical accuracy in regulatory submissions and product development decisions.

  • Present updates, outcomes, and key issues to senior management.


Required Qualifications

  • Bachelor’s degree in Statistics or Mathematics.

  • Master’s degree with 5+ years of related experience, or PhD with 3+ years of related experience (preferred).

  • Demonstrated expertise in statistical programming, clinical trial methodology, and regulatory documentation.

  • Strong communication skills for presenting complex statistical concepts to technical and non-technical stakeholders.

  • Ability to manage multiple priorities and deliver high-quality outputs within defined timelines.


Compensation

Base Salary Range:
USD 86,700 – 173,300 annually
(Compensation may vary based on location and relevant experience.)


Why Join Abbott

Abbott supports career progression, scientific excellence, and employee wellbeing through:

  • Global career development and advancement pathways.

  • Eligibility for free medical coverage through the Health Investment Plan (HIP) PPO (subject to program rules).

  • Strong retirement savings plan with a competitive employer contribution.

  • Tuition reimbursement and educational programs such as Freedom 2 Save and FreeU.

  • Recognition as one of the world’s most admired companies and a leading employer for diversity and scientific talent.