Design, implement, interpret, report and publish the results of retrospective and prospective observational research studies for life sciences customers
Support the development of N-Power Medicine’s data platform and assets, including specification of data models and clinical nomenclature/coding requirements to efficiently harmonize real-world data with clinical trials data standards, such as Clinical Data -Interchange Standards Consortium (CDISC)
Contribute to developing N-Power Medicine’s real-world evidence generation platform, in alignment with the company’s by-protocol, prospective real-time data
Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the company's strategic partnerships with life sciences
Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the data requirements to support N-Power Medicine’s next-generation External Controls methodology and product offerings
Help translate the perspectives and requirements of FDA and regulatory agencies around external controls to inform N-Power Medicine's data capture/collection and platform requirements
Ask the right scientific questions, ideate and make recommendations on fit-for-purpose data and analytics solutions
Stay current with novel data analysis methods for observational data, in particular Causal Inference and its applications to clinical trials
Perform additional duties and responsibilities as required

Requirements

10+ years of experience with a Master’s Degree and 5+ with a PhD in Epidemiology, Biostatistics or a Related field
Oncology experience strongly preferred
Knowledge of RWD study design and execution, particularly causal inference
Experience with data analysis, specifically from observational study designs
Experience with epidemiological, registry, EMR, clinical trials, and other clinical data
Experience using R, Python, SQL or similar and a highly technical acumen
Experience summarizing data and disseminating insights to multi-disciplinary audiences
Experience with managing timelines, and relationships with key stakeholders
Confident in presenting the N-Power brand in scientific conferences and other professional forums
Understanding of drug development, regulatory requirements and processes
You are a doer, self motivated, and driven
Comfortable within a growth stage environment
Effective scientific communication; written and verbal
Strong publication history, and teaching/mentoring experience is preferred
Generous, Curious, and Humble

Benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

data analysisobservational study designcausal inferenceepidemiologybiostatisticsRPythonSQLclinical datadata modeling

Soft Skills

scientific communicationpresentation skillsrelationship managementself-motivateddrivencollaborationcuriosityhumilityteachingmentoring