Salary
💰 $195,000 - $230,000 per year
About the role
- Responsible for statistical activities in support of Medical Affairs, including design, execution, interpretation, and communication of analyses that inform medical decision-making, health outcomes, and scientific exchange
- Contribute scientific and methodological expertise to support medical strategy, publications, and external engagements
- Interact with internal and external cross-functional study teams and support interactions with the medical community
- Manage CRO programmers and statisticians in preparing analysis files and performing statistical analyses; set expectations on deliverables and timelines and ensure accuracy and timeliness of deliverables
- Provide statistical input to medical publications, scientific congresses, and external collaborations
- Apply appropriate statistical methodologies supporting medical insights, value demonstration, safety monitoring, and lifecycle management
- Ensure high-quality statistical deliverables that meet scientific and regulatory standards
- Partner with colleagues in Medical Affairs, HEOR, Clinical Development, and other cross-functional teams to align statistical activities
- Translate statistical concepts into clear insights for medical and scientific stakeholders
- Stay current with evolving statistical methods, data sources, and regulatory expectations related to real-world evidence
Requirements
- PhD or Master’s degree in Biostatistics, Statistics, or related field
- 7+ years (PhD) or 10+ years (Master’s) of biostatistics experience in the pharmaceutical/biotech industry
- Strong knowledge of statistical methodologies, current drug development trends, and regulatory environments
- Strong analytical and problem-solving skills; able to identify and investigate issues and causes independently and formulate potential solutions
- Excellent written and verbal communication skills, with the ability to engage both technical and non-technical audiences
- Excellent programming skills in SAS and/or R
- Ability to work as a part of a cross-functional team in a fast-paced environment and to work collaboratively with external partners and vendors
- Experience contributing to medical publications and scientific communications preferred
- Familiarity with HEOR and real-world evidence analysis preferred