Senior Manager, Biostatistics

Insmed Incorporated•NJ Corporate Headquarters, NJ

3d•Remote

About The Position

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? About the Role: We’re looking for a Senior Manager, Biostatistics on the Biometrics team to help us expand what’s possible for patients with serious diseases. Reporting to the Senior Director, Biostatistics, you’ll provide statistical expertise for clinical trial(s) within one or more compounds in development. You will support the design, setup, execution, analysis, and reporting of clinical studies, and contribute as a key member of cross-functional teams. The position requires solid technical and communication skills, and the ability to work independently with moderate guidance.

Requirements

PhD in Statistics/Biostatistics
2+ years of relevant pharmaceutical experience
Strong knowledge of statistical concepts and techniques commonly used in clinical development
Familiarity with regulatory requirements and guidelines for clinical research
Comprehensive knowledge and understanding of advanced statistical concepts and techniques applicable to clinical research
Excellent project management, interpersonal and communication skills
Ability to work independently, manage multiple priorities, and collaborate effectively in a team environment

Responsibilities

Provide statistical input into protocol development, statistical analysis plans, and other key trial documents.
Support study setup activities including randomization, sample size justification, and selection of appropriate analysis methods.
Perform or oversee statistical analyses of clinical trial data to ensure timely and accurate reporting.
Contribute to the preparation of clinical study reports, regulatory submissions, and responses to health authority queries.
Collaborate with cross-functional teams (clinical, programming, data management, regulatory) to ensure statistical integrity and compliance.
Review and provide feedback on deliverables from CRO partners or internal programming teams.
Assist in the development and implementation of departmental standards and infrastructure initiatives.
Stay current with relevant statistical methodology and regulatory guidance, and apply as appropriate.

Benefits

Comprehensive medical, dental, and vision coverage
Mental health support
Annual wellbeing reimbursement
Access to our Employee Assistance Program (EAP)
Generous paid time off policies
Fertility and family-forming benefits
Caregiver support
Flexible work schedules
401(k) plan with a competitive company match
Annual equity awards
Participation in our Employee Stock Purchase Plan (ESPP)
Company-paid life and disability insurance
Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities
Employee resource groups
Service and recognition programs
Meaningful opportunities to connect, volunteer, and give back