Senior Staff Biostatistician (Remote)

Lensa; Boston (MA); Remote; USD 100,000 - 216,000; Full time

Job summary

A leading medical device company is seeking a Senior Staff Biostatistician to lead statistical strategy for clinical trials. This remote role involves ensuring regulatory readiness and advancing patient care through data-driven insights. Candidates should have a strong background in biostatistics and clinical trial analysis.

Benefits

Medical, dental, and vision insurance

401(k) plan

Stock purchase plan

Wellness programs

Qualifications

• 6+ years of experience in clinical biostatistics.
• Proficiency in SAS programming.
• Experience with regulatory documentation.

Responsibilities

• Lead statistical planning and analysis for clinical trials.
• Design and validate SAS programs for clinical datasets.
• Collaborate with cross-functional teams on study design.

Skills

SAS programming

Clinical trial data analysis

Inferential statistics

Statistical concepts communication

Education

Bachelor’s degree in Biostatistics, Engineering, Science, or related field

Tools

SAS

SQL

R programming

Job description

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Lensa is the leading career site for job seekers at every stage of their career. Our client, Stryker, is seeking professionals. Apply via Lensa today!

Stryker Neurovascular is seeking a Senior Staff Biostatistician to lead statistical strategy and execution for clinical trials supporting innovative neurointerventional medical devices. In this role, you will play a critical part in shaping clinical evidence, ensuring regulatory readiness, and advancing patient care through data-driven insights. This is a remote position to be located anywhere within the United States, preferably on the Central or Eastern time zone.

What You Will Do

• Lead statistical planning and analysis for clinical trials, including development of statistical analysis plans (SAPs) and interpretation of complex data
• Design and validate SAS programs to generate clinical datasets, tables, listings, and figures (TLGs) in compliance with regulatory standards
• Collaborate with cross-functional teams—including clinical scientists, regulatory affairs, and neurointerventional physicians—to optimize study design and endpoints
• Provide statistical input for regulatory submissions (e.g., FDA, EU MDR) and support clinical study reports (CSRs)
• Contribute to scientific publications and conference presentations to communicate clinical evidence
• Ensure statistical best practices across projects
• Stay current with evolving regulatory guidance and statistical methodologies relevant to medical devices

Required

What you need

• Bachelor’s degree in Biostatistics, Engineering, Science, or related field
• 6+ years of experience in clinical biostatistics
• Proficiency in SAS programming; strong ability to communicate statistical concepts to non-statisticians
• Experience with clinical trial data analysis, inferential statistics, and regulatory documentation

Preferred

• MS or PhD in Statistics, Mathematics, or related field
• 4+ years in medical device, pharmaceutical, or biotech settings
• Experience with SQL, SAS Macros, and electronic data capture (EDC) systems
• Experience in R programming
• Prior contributions to peer-reviewed publications or scientific presentations
• Familiarity with ISO 14155, FDA guidance, and EU MDR requirements

Salary range: $100,500 - $215,300 plus bonus and benefits. Actual salary may vary based on location, skills, and experience.

Benefits include medical, dental, vision, critical illness, accident, hospital indemnity insurance, HSA, FSA, 401(k), stock purchase plan, life and disability insurance, and wellness programs.

Stryker is an equal opportunity employer. Qualified applicants will receive consideration without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or veteran status.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Research, Analysis, IT
• Industries: IT Services and Consulting