Top Tech Jobs & Startup Jobs in Chicago, IL

Lead statistical programming for multiple clinical development projects, ensuring quality and compliance while collaborating with cross-functional teams and overseeing data analysis.

The Director will manage global regulatory strategies and processes, provide leadership on regulatory issues, and interface with business partners and regulatory authorities to secure product approvals and market access.

The Regional Clinical Study Senior Manager is responsible for overseeing regional study delivery, managing clinical operations teams, ensuring compliance with quality standards, and collaborating with stakeholders on study progress and strategy.

The Associate Director will enhance risk management, compliance, and security measures. Responsibilities include developing policies, managing third-party risks, and leading GRC implementations across North America & LATAM.

Summer internship supporting people analytics: clean and analyze employee survey data, build predictive models (attrition, engagement), create dashboards and narratives, and automate reporting to inform HR decisions.

Lead global commercial strategy for early hematology pipeline: provide commercial input to R&D and Early Development Teams, develop TEPs/TPPs, size market opportunities, define evidence and reimbursement needs, guide portfolio valuation and investment decisions, and align cross-functional stakeholders to drive product development and launch readiness.

Lead design and delivery of enterprise-scale solutions on internal low-code platforms. Drive discovery, define solution architecture, ensure security/compliance, support POCs and implementations, mentor engineers, and enable stakeholder adoption and handover.

Summer internship supporting Global Quality by identifying, collecting, and categorizing data; performing basic statistical analysis; designing dashboards and charts (Excel/Power BI); coordinating data collection with global Quality teams; and performing minor administrative tasks.

The position involves managing IP portfolios, conducting patent analysis, supporting corporate development, and providing litigation support in the biopharmaceutical industry.

Lead GPMS operations and governance for global publications, manage medical communications projects end-to-end, support database maintenance and vendor enhancements, ensure SOP and Good Publication Practices compliance, provide onboarding/training, support audits and metric reporting, and develop cross-functional communications.