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Senior Staff Biostatistician (Remote)

Stryker

United (PA)

Remote

USD 100,000 - 216,000

Full time

Yesterday
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Job summary

A leading medical device company is seeking a Senior Staff Biostatistician to lead statistical strategy for clinical trials. This remote position requires expertise in SAS programming and clinical biostatistics, with a focus on innovative neurointerventional medical devices. The role involves collaboration with teams to ensure best practices and contribute to scientific publications. Competitive salary and benefits are offered based on experience.

Benefits

Health Insurance
Dental Insurance
Vision Insurance
401(k)
Stock Purchase Plans
Wellness Programs

Qualifications

  • 6+ years of experience in clinical biostatistics.
  • Experience with clinical trial data analysis and regulatory documentation.

Responsibilities

  • Lead statistical planning and analysis for clinical trials.
  • Collaborate with cross-functional teams to optimize study design.
  • Provide statistical input for regulatory submissions.

Skills

SAS Programming
Statistical Analysis
Communication

Education

Bachelor’s degree in Biostatistics
MS or PhD in Statistics

Tools

SQL
SAS Macros
R Programming

Job description

Join to apply for the Senior Staff Biostatistician (Remote) role at Stryker

Job Overview

Stryker Neurovascular is seeking a Senior Staff Biostatistician to lead statistical strategy and execution for clinical trials supporting innovative neurointerventional medical devices. This remote position can be based anywhere in the United States, preferably in the Central or Eastern time zones.

Responsibilities
  1. Lead statistical planning and analysis for clinical trials, including development of SAPs and data interpretation.
  2. Design and validate SAS programs for clinical datasets, tables, listings, and figures (TLGs) in compliance with regulatory standards.
  3. Collaborate with cross-functional teams to optimize study design and endpoints.
  4. Provide statistical input for regulatory submissions and support clinical study reports.
  5. Contribute to scientific publications and conference presentations.
  6. Ensure statistical best practices across projects.
  7. Stay updated with regulatory guidance and statistical methodologies relevant to medical devices.
Minimum Requirements
  • Bachelor’s degree in Biostatistics, Engineering, Science, or related field.
  • 6+ years of experience in clinical biostatistics.
  • Proficiency in SAS programming and ability to communicate statistical concepts effectively.
  • Experience with clinical trial data analysis, inferential statistics, and regulatory documentation.
Preferred Qualifications
  • MS or PhD in Statistics, Mathematics, or related field.
  • 4+ years in medical device, pharmaceutical, or biotech sectors.
  • Experience with SQL, SAS Macros, EDC systems, and R programming.
  • Contributions to peer-reviewed publications or scientific presentations.
  • Knowledge of ISO 14155, FDA guidance, and EU MDR requirements.
Compensation & Benefits

Salary ranges from $100,500 to $215,300 plus bonuses and benefits, with actual figures based on experience and location. Benefits include health, dental, vision, HSA, FSA, 401(k), stock purchase plans, insurance, and wellness programs.

Additional Details
  • Seniority level: Mid-Senior level
  • Employment type: Full-time
  • Job functions: Research, Analysis, IT
  • Industries: Medical Equipment Manufacturing, etc.
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