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Epidemiology Director

2 months, 2 weeks ago
United States
Full-time
Lead
Data Scientist
Data Science and Analytics
Python R SQL
Apply Now
N-Power Medicine

N-Power Medicine

N-Power Medicine accelerates drug development by creating a research-ready network that integrates standard of care patients and diverse populations into clinical trials, facilitating informed decision-making for phase II to phase III studies in oncology.

Biotechnology
11-50
Founded 2021
View All Jobs 6

Description

  • Design, implement, interpret, report, and publish retrospective and prospective observational research studies for life sciences customers.
  • Support development of the data platform and assets by defining data models and clinical nomenclature/coding requirements.
  • Help harmonize real-world data with clinical trial data standards such as CDISC.
  • Contribute to the real-world evidence generation platform aligned with by-protocol, prospective real-time data.
  • Collaborate with Clinical Science, Commercial, and Network Partners on strategic life sciences partnerships.
  • Collaborate with internal partners to define data requirements for next-generation External Controls methodology and product offerings.
  • Translate FDA and regulatory perspectives on external controls into data capture, collection, and platform requirements.
  • Ask scientific questions and recommend fit-for-purpose data and analytics solutions.
  • Stay current on novel observational data analysis methods, especially causal inference and its clinical trial applications.
  • Perform additional duties and responsibilities as required.

Requirements

  • 10+ years of experience with a Master’s degree, or 5+ years with a PhD, in Epidemiology, Biostatistics, or a related field.
  • Oncology experience is strongly preferred.
  • Knowledge of real-world data study design and execution, particularly causal inference.
  • Experience with data analysis from observational study designs.
  • Experience with epidemiological, registry, EMR, clinical trials, and other clinical data.
  • Experience using R, Python, SQL, or similar tools, with strong technical acumen.
  • Experience summarizing data and communicating insights to multidisciplinary audiences.
  • Experience managing timelines and relationships with key stakeholders.
  • Understanding of drug development, regulatory requirements, and processes.
  • Strong publication history; teaching or mentoring experience is preferred.
  • Ability to travel from time to time.
  • Must be currently authorized to work in the U.S. on a full-time basis; visa sponsorship is not provided.

Benefits

  • Competitive salary range of $165,000 to $248,000.
  • Equity at hire.
  • Discretionary annual bonus based on company performance.
  • Eligible for company benefits.
  • Balanced and flexible work environment.
  • Competitive industry benefits.
  • 401(k) plan.
  • Other company perks.

Interested in this position?

Apply directly on the company website

Apply Now

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