Associate Director, Biostatistician
Madrigal Pharmaceuticals
17 days ago
Remote friendly (Conshohocken, PA)
United States
Clinical Research and Development
Associate Director of Biostatistics
Responsibilities:
- Independently lead statistical modeling and analyses for assigned studies/projects in coordination with senior biostatisticians, programmers, and cross-functional teams.
- Perform and review complex statistical analyses; contribute to protocol development; prepare Statistical Analysis Plans as needed.
- Lead analysis efforts of 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 4–5 years of experience, or Master’s degree with 7+ years in a Pharma/Biotech environment.
- Experience designing and analyzing clinical trials and healthcare datasets.
- Solid foundation in advanced statistical methods and computing (R, SAS).
- Ability to communicate complex statistical analyses/concepts to non-statisticians.
- Knowledge of regulatory guidelines in pharmaceutical development.
- Excellent organizational and communication skills.
Skills/Knowledge (expected):
- Working knowledge of clinical data structures (SDTM/ADaM), data management workflows, and statistical programming languages (SAS and/or R).
Benefits (explicitly stated):
- Base pay, bonus, equity; flexible paid time off; medical/dental/vision and life/disability insurance; 401(k) options; supplemental life insurance and legal services; Employee Assistance Program mental health benefits.
Application instructions:
- Apply via the Madrigal Careers site on an ongoing basis.
Responsibilities:
- Independently lead statistical modeling and analyses for assigned studies/projects in coordination with senior biostatisticians, programmers, and cross-functional teams.
- Perform and review complex statistical analyses; contribute to protocol development; prepare Statistical Analysis Plans as needed.
- Lead analysis efforts of 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 4–5 years of experience, or Master’s degree with 7+ years in a Pharma/Biotech environment.
- Experience designing and analyzing clinical trials and healthcare datasets.
- Solid foundation in advanced statistical methods and computing (R, SAS).
- Ability to communicate complex statistical analyses/concepts to non-statisticians.
- Knowledge of regulatory guidelines in pharmaceutical development.
- Excellent organizational and communication skills.
Skills/Knowledge (expected):
- Working knowledge of clinical data structures (SDTM/ADaM), data management workflows, and statistical programming languages (SAS and/or R).
Benefits (explicitly stated):
- Base pay, bonus, equity; flexible paid time off; medical/dental/vision and life/disability insurance; 401(k) options; supplemental life insurance and legal services; Employee Assistance Program mental health benefits.
Application instructions:
- Apply via the Madrigal Careers site on an ongoing basis.