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Manager, Programming Infrastructure & Analytics Enablement

Insmed Incorporated

Any City, USRemotePosted 5 days ago$133,000 - $173,000/year
Full TimeSenior LevelBioinformatics & Data SciencePharmaceutical
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Summary

We're looking for a Manager, Programming Infrastructure & Analytics Enablement on the Programming team to help us expand what's possible for patients with serious diseases. Reporting to the Sr Director, Programming Infrastructure & Analytics Enablement, you'll develop, implement, maintain, and optimize data analytics solutions that support the strategic vision of Programming by using relevant technologies and tools. You will also work with internal partners, as well as cross-functional stakeholders to understand business needs and develop technical solutions.

Job description

About the Role

We're looking for a Manager, Programming Infrastructure & Analytics Enablement on the Programming team to help us expand what's possible for patients with serious diseases. Reporting to the Sr Director, Programming Infrastructure & Analytics Enablement, you'll develop, implement, maintain, and optimize data analytics solutions that support the strategic vision of Programming by using relevant technologies and tools. You will also work with internal partners, as well as cross-functional stakeholders to understand business needs and develop technical solutions.

What You'll Do

In this role, you'll have the opportunity to support analysis and reporting of clinical trial and related data by developing and maintaining automated processes/tools/solutions that boost efficiency, increase throughput and preserve quality and compliance, in support of the Biometrics infrastructure and analytics platform strategy.

  • Identify gaps and then develop, test, implement and maintain technical solutions such as Packages/Utilities/Macros that accelerate statistical programming of clinical trial data
  • Contribute to identifying and onboarding technologies/tools/platforms that support current and future data analytics/visualization needs, including hands-on evaluation and piloting of new solutions
  • Engage with stakeholders to gather requirements and propose technical solutions that leverage existing capabilities, supporting automation and standardization
  • Lead technical implementation of assigned projects/workstreams, including creation of proof-of-concepts and contributing to solution designs
  • Manage assigned initiatives to meet team objectives with moderate supervision, prioritizing own work and support planning within the team
  • Support the management of clinical trial data and other stakeholder data to ensure efficient storage/archival/retrieval/reporting, while supporting data integrity, security, and regulatory compliance
  • Execute change management activities during the maintenance and upgrades of systems/tools/processes, ensuring adherence to computer system validation (CSV) requirements and quality standards
  • Provide technical guidance, training, and user support to maximize adoption of technical solutions and stakeholder satisfaction, while staying current on emerging data analytics techniques and pursuing professional development to strengthen technical, scientific, and operational capabilities in line with policies and regulatory standards

Who You Are

You have a Bachelor's degree in Biostatistics, Statistics, Computer Science, Data Science, or a related field, with 5+ years of relevant experience; or an advanced degree (MS) in a related discipline with 3+ years of experience in statistical programming and analytics within pharmaceutical or biotechnology clinical development.

  • Strong proficiency in R required, with familiarity with the pharmaverse and tidyverse ecosystems for clinical data analysis and reporting
  • Working knowledge of CDISC standards and clinical trial data structures, with demonstrated ability to develop and maintain reusable programming utilities, macros, and packages
  • Demonstrated ability to manage multiple projects/tasks simultaneously, delivering on agreed timelines and escalating risks to management and stakeholders as needed
  • Strong collaborative, proactive problem-solver with sound decision-making, effective both independently and in cross-functional team environments
  • Excellent verbal and written communication skills, highly organized with strong attention to detail, clarity, and accuracy
  • Forward-looking thinker who identifies opportunities and contributes ideas for process and technical improvement

Nice to Have (but not required)

  • Experience with SAS, Python, and R package development are pluses
  • Experience with version control (e.g. Git); familiarity with CI/CD pipelines and cloud platforms is a plus

Where You'll Work

This is a fully remote role. It can be performed effectively from anywhere while staying connected to your Insmed team and community. Occasional travel for team meetings or events will be expected. Minimal travel expected.

Requirements

  • Bachelor's degree in Biostatistics, Statistics, Computer Science, Data Science, or related field with 5+ years of relevant experience; or advanced degree (MS) with 3+ years of statistical programming and analytics experience in pharmaceutical or biotechnology clinical development
  • Strong proficiency in R required
  • Familiarity with pharmaverse and tidyverse ecosystems for clinical data analysis and reporting
  • Working knowledge of CDISC standards and clinical trial data structures
  • Demonstrated ability to develop and maintain reusable programming utilities, macros, and packages
  • Demonstrated ability to manage multiple projects/tasks simultaneously, delivering on agreed timelines and escalating risks
  • Strong collaborative, proactive problem-solver with sound decision-making
  • Effective both independently and in cross-functional team environments
  • Excellent verbal and written communication skills
  • Highly organized with strong attention to detail, clarity, and accuracy
  • Forward-looking thinker who identifies opportunities and contributes ideas for process and technical improvement

Benefits

  • Medical, Dental & Vision
  • Mental Health Support
  • Wellbeing Reimbursement
  • Employee Assistance Program
  • Generous Paid Time Off
  • Fertility & Family-Forming Benefits
  • Caregiver Support
  • Flexible Work Schedules
  • 401(k) Matching
  • Annual Equity Awards
  • Employee Stock Purchase Plan
  • Life & Disability Insurance
  • LinkedIn Learning Access
  • Skill Building Workshops
  • Leadership Programs
  • Mentorship Connections
  • Employee Resource Groups

Company overview

Insmed Incorporated is a people-first global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases. Headquartered in Bridgewater, New Jersey, with offices and research locations throughout the United States, Europe, and Japan, the company focuses on delivering first- and best-in-class therapies for underserved patient communities. Insmed's portfolio includes two approved therapies for chronic lung diseases: ARIKAYCE for Mycobacterium avium complex lung disease and BRINSUPRI for non-cystic fibrosis bronchiectasis. The company is advancing a diverse pipeline of mid- to late-stage investigational medicines and cutting-edge drug discovery programs spanning gene therapy, AI-driven protein engineering, RNA end-joining, and synthetic rescue technologies. Recognized as the No. 1 Science Top Employer for five consecutive years, Insmed employs 1,001-5,000 professionals globally and maintains a strong commitment to innovation, patient-centricity, and corporate responsibility.

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