Regulatory Biostatistician — Clinical Trials & Submissions

UNAVAILABLE; Boston (MA); On-site; USD 210,000 - 255,000; Full time

Benefits offered by this job

Comprehensive benefits package

Discretionary annual bonus

Job summary

Analysis Group is seeking an experienced Biostatistician in Boston to support clinical trial and biostatistics capabilities. Candidates should possess strong skills in clinical trial data, statistical programming, and regulatory processes.

The role involves leading analytical workstreams, mentoring analysts, and contributing to strategic decision-making in a diverse portfolio of client engagements, with expertise in biostatistical methods and clinical development.

Qualifications

• Advanced degree required (PhD preferred, Master’s considered) in Biostatistics or related field.
• Minimum of 3 years of relevant experience required.
• Experience in clinical trials, pharmaceutical, biotech, or CRO environments.

Responsibilities

• Apply biostatistical methods for clinical development and regulatory submissions.
• Contribute to strategic advising on clinical trial design.
• Manage and mentor teams of analysts and associates.

Skills

Biostatistics

Statistical programming

Clinical trial design

Regulatory submissions

Problem-solving

Communication skills

Education

PhD in Biostatistics, Statistics, or related field

Master's degree in a quantitative field

Job description

Analysis Group is seeking an experienced Biostatistician in Boston to support clinical trial and biostatistics capabilities. Candidates should possess strong skills in clinical trial data, statistical programming, and regulatory processes.

The role involves leading analytical workstreams, mentoring analysts, and contributing to strategic decision-making in a diverse portfolio of client engagements, with expertise in biostatistical methods and clinical development.