Originate, expand, and retain client relationships; meet or exceed annual personal sales and delivery targets; lead pursuit strategy, scoping, and pricing.
Serve as consulting expert and testifying expert in litigation and regulatory matters (depositions, reports, oral testimony).
Support epidemiological analyses across environmental, occupational, regulatory, and health sciences projects.
Conduct literature reviews, assist with protocol development, data management, and statistical analyses (R, SAS, Stata, SPSS, or Python).
Draft supporting sections of reports, research summaries, and client deliverables.
J.S. Held is a global consulting firm that combines technical, scientific, financial, and strategic expertise to advise clients seeking to realize value and mitigate risk. They provide a comprehensive suite of services, products, and data that enable clients to navigate complex, contentious, and often catastrophic situations.
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
Contribute to developing N-Power Medicine’s real-world evidence generation platform, in alignment with the company’s by-protocol, prospective real-time data
N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. They are a mission-driven, well-funded, rapidly growing company, eager to attract passionate professionals.