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As a Senior Clinical Research Associate, you will monitor clinical trial sites, ensure compliance with protocols, and support site personnel in executing trials. Your role includes managing multiple sites, training staff, and upholding data integrity throughout the study lifecycle.

The Supplier Performance Manager will manage supplier-specific objectives, coordinate projects, foster relationships, and oversee vendor activities in clinical research.

As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements while managing site performance and collaborating with cross-functional teams.

The Site Specialist II role involves supporting regulatory documentation, ensuring compliance for site activation, and collaborating with stakeholders for optimal study performance.

Monitor clinical trial sites for compliance, conduct site visits, manage multiple projects, train site staff, and ensure data integrity in ophthalmology studies.

As a Clinical Research Associate, you will conduct various trial visits, ensure protocol compliance, and collaborate with investigators to maintain data integrity and patient safety.

Manage day-to-day operations of clinical trials, ensure compliance with regulations, oversee trial teams, budget management, and vendor interactions.

The Feasibility Informatics Manager leads clinical project feasibility, providing strategic input and delivering feasibility studies on time and on budget, collaborating with cross-functional teams to ensure high-quality outcomes.

The Local Trial Manager is responsible for coordinating clinical trials, ensuring compliance, managing budgets, overseeing local study teams, and interacting with various stakeholders for successful study execution.

Oversee site contracts for clinical studies, manage contract development, collaborate with teams, ensure financial management, and mentor others.