Quantitative Data Analyst, Flatiron Health

• You hold a Master’s degree with 1-3 years of experience or Bachelors degree with 3-5 years of experience. Relevant disciplines include public health, epidemiology, or biostatistics
• You are an effective communicator, with experience drafting and developing complex, technical documentation
• You know how to balance attention to detail with execution against tight timelines, and you are capable of managing multiple high-visibility projects simultaneously
• You love working with data and have experience exploring it with a critical and thoughtful eye
• You are proficient in R (or another programming language and are committed to becoming an expert in R)
• You are self-motivated, flexible, proactive and enjoy coming up with elegant and innovative solutions to challenging problems
• You are passionate about our mission to improve healthcare through technology

Desirable

• In this role, you will work as a member of the Quantitative Sciences (QS) department, primarily supporting the Custom Solutions and Services (CSS) team within the Client Solutions organization
• This team provides custom real-world data and analytics solutions to address the most important research questions across clinical development, market access, and commercial use cases for our life sciences partners
• Xecute literature reviews and exploratory data analysis to inform study design & cross-functional decision-making
• Working closely with study leads, lead development of high quality, readily interpretable internal and client-facing protocols and statistical analysis plans
• Partner with statistical programmers to ensure accurate implementation of analyses in accordance with study plans
• Interpret and summarize study findings in high quality, readily interpretable study reports, presentations, and other relevant client-facing deliverables, for review by study leads
• Work collaboratively with cross-functional stakeholders across Quantitative Sciences, Research Oncology, Regulatory Affairs, and Life Science Partnerships to execute and deliver on projects in an accurate, effective, and timely manner
• Adhere to all research publication, regulatory, and authorship standards (e,g. ICMJE, GPP4, ICH E3, ICH E6, ICH E9, HIPAA, GPP and GCP) and comply with internal processes
• Contribute to client-facing meetings
• Consult with Medical Writing to identify scientific content requiring standardization and contribute to efforts to develop and enhance templates for client-facing scientific writing deliverables
• Continue to develop a deeper understanding of real-world data and related methodologies used to generate real-world evidence