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Associate Biostatistician

Abbott
Abbott
1+ years
$81,500.00 – $141,300.00
10 Jan. 6, 2026
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

Associate Biostatistician – Medical Device Clinical Research

Location: Maple Grove, MN | Santa Clara, CA | Burlington, MA (Onsite)
Category: Medical & Clinical Affairs
Experience Required: Minimum 1 year in biostatistics or related field
Employment Type: Full-time | Onsite


Company Overview

Abbott is a global healthcare leader dedicated to improving lives through innovative medical technologies. With more than 114,000 employees across 160+ countries, Abbott delivers world-class solutions in diagnostics, medical devices, nutrition, and branded generics. Abbott is consistently recognized as a top employer for diversity, innovation, and scientific excellence.


Role Overview

Abbott’s Medical Device Clinical Research organization is seeking a detail-oriented Associate Biostatistician to provide statistical support for clinical studies. This role involves designing study protocols, creating statistical analysis plans, performing statistical analyses, generating tables and reports, and ensuring data integrity across all projects.

The Associate Biostatistician works under the supervision of a statistical manager and collaborates with cross-functional clinical study teams to ensure high-quality, accurate, and compliant statistical outcomes.


Key Responsibilities

  • Review clinical study protocols and provide statistical input.

  • Assist in implementing statistical analysis plans and study methodologies.

  • Ensure accuracy and timeliness of statistical input in reports and decisions.

  • Develop, document, and validate computer programs for data analysis.

  • Generate, validate, and review datasets, tables, listings, and figures.

  • Identify and correct inconsistencies or errors in statistical reporting and interpretation.

  • Provide support and insights for non-standard questions from internal or external stakeholders.

  • Support the development of CRFs, study schemas, and reporting structures per project timelines.

  • Ensure compliance with Abbott quality systems and maintain high documentation standards.

  • Communicate basic clinical principles and provide formal statistical guidance to non-statisticians.

  • Escalate critical issues or deviations to supervisors promptly.


Education & Experience

Required Qualifications:

  • Bachelor’s degree in Statistics, Mathematics, or a related field.

  • Minimum 1 year of relevant experience in biostatistics or clinical research.

Preferred Qualifications:

  • Master’s or PhD in Statistics, Biostatistics, or related scientific discipline.

  • Experience supporting medical device clinical trials or regulated environments.

  • Proficiency in statistical software (SAS, R, or equivalent).

  • Strong analytical, problem-solving, and communication skills.


Why Join Abbott

  • Opportunity to work on innovative medical device research in a globally recognized organization.

  • Access to comprehensive career development and training programs.

  • Competitive compensation with base pay of $81,500 – $141,300, depending on experience and location.

  • Health, wellness, and retirement benefits including medical, dental, vision, 401(k) matching, and tuition assistance.

  • Dynamic, collaborative work environment with focus on safety, compliance, and professional growth.