Senior Manager, Biostatistics

Insmed; New York (NY); Remote; USD 133,000 - 173,000; Full time

Job summary

Insmed seeks a Senior Manager of Biostatistics to provide statistical expertise for clinical trials within its biopharmaceutical development pipeline. This fully remote position supports protocol development, trial analysis, and regulatory submissions as a key member of cross-functional teams.

The role requires a PhD in Statistics or Biostatistics and at least two years of pharmaceutical or clinical development experience, with strong knowledge of statistical concepts, regulatory guidelines, and

Qualifications

• PhD in Statistics or Biostatistics required.
• 2+ years in pharmaceutical or clinical development.
• Strong knowledge of statistical concepts in clinical development.
• Familiarity with regulatory requirements and clinical research guidelines.
• Excellent communication and interpersonal skills.

Responsibilities

• Provide statistical input into protocol development, analysis plans, and trial documents.
• Support study setup including randomization, sample size justification, and analysis method selection.
• Perform or oversee statistical analyses of clinical trial data for accurate reporting.
• Contribute to clinical study reports, regulatory submissions, and health authority responses.
• Collaborate with cross-functional teams to ensure statistical integrity and compliance.

Skills

Statistical analysis

Communication

Project management

Independent work

Education

PhD in Statistics or Biostatistics

Job description

Insmed seeks a Senior Manager of Biostatistics to provide statistical expertise for clinical trials within their biopharmaceutical development pipeline. This fully remote position supports protocol development, trial analysis, and regulatory submissions as a key member of cross-functional teams.

Responsibilities

• Provide statistical input into protocol development, analysis plans, and trial documents
• Support study setup including randomization, sample size justification, and analysis method selection
• Perform or oversee statistical analyses of clinical trial data for accurate reporting
• Contribute to clinical study reports, regulatory submissions, and health authority responses
• Collaborate with cross-functional teams to ensure statistical integrity and compliance

Requirements

• PhD in Statistics or Biostatistics
• 2+ years pharmaceutical or clinical development experience
• Strong knowledge of statistical concepts in clinical development
• Familiarity with regulatory requirements and clinical research guidelines
• Advanced statistical concepts and techniques applicable to clinical research
• Excellent project management, communication, and interpersonal skills
• Ability to work independently and manage multiple priorities

Compensation: $133,000-$173,000 annual