Senior Biostatistician
Madrigal Pharmaceuticals
August 12, 2026
Remote friendly (Conshohocken, PA)
United States
Clinical Research and Development
Responsibilities:
- Execute statistical modeling and analyses, coordinating with biostatisticians, programmers, and cross-functional team members to meet R&D objectives.
- Perform and review complex statistical analyses; contribute to protocol development and prepare Statistical Analysis Plans as needed.
- Design and analyze clinical and real-world data to support evidence generation from randomized trials and observational studies.
- Establish effective collaborations with cross-functional teams (clinical research, medical affairs, clinical operations, data management).
- Contribute to scientific excellence through statistical innovation and participation in external conferences.
Qualifications:
- Ph.D. in (Bio)statistics with 2+ yearsβ experience, or Masterβs degree with 5+ yearsβ experience in a Pharma or Biotech environment.
- Experience in design and analysis of clinical trials and healthcare datasets.
- Solid foundation in advanced statistical methods and computing (R, SAS).
- Ability to communicate complex statistical analyses and concepts to non-statisticians.
- Knowledge of regulatory guidelines in pharmaceutical development (plus).
- Excellent organizational and communication skills.
Benefits:
- Full-time employees are eligible for comprehensive benefits including flexible paid time off, medical, dental, vision, life/disability insurance, and 401(k) offerings.
Application instructions:
- Applications accepted on an ongoing basis via the Madrigal Careers site.
- Execute statistical modeling and analyses, coordinating with biostatisticians, programmers, and cross-functional team members to meet R&D objectives.
- Perform and review complex statistical analyses; contribute to protocol development and prepare Statistical Analysis Plans as needed.
- Design and analyze clinical and real-world data to support evidence generation from randomized trials and observational studies.
- Establish effective collaborations with cross-functional teams (clinical research, medical affairs, clinical operations, data management).
- Contribute to scientific excellence through statistical innovation and participation in external conferences.
Qualifications:
- Ph.D. in (Bio)statistics with 2+ yearsβ experience, or Masterβs degree with 5+ yearsβ experience in a Pharma or Biotech environment.
- Experience in design and analysis of clinical trials and healthcare datasets.
- Solid foundation in advanced statistical methods and computing (R, SAS).
- Ability to communicate complex statistical analyses and concepts to non-statisticians.
- Knowledge of regulatory guidelines in pharmaceutical development (plus).
- Excellent organizational and communication skills.
Benefits:
- Full-time employees are eligible for comprehensive benefits including flexible paid time off, medical, dental, vision, life/disability insurance, and 401(k) offerings.
Application instructions:
- Applications accepted on an ongoing basis via the Madrigal Careers site.