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As a Clinical Research Associate II, you will monitor clinical trial sites, support investigators, ensure compliance, and manage study data, contributing to healthcare improvements.

The AI Solution Developer will leverage Palantir Foundry to create AI-driven solutions, design ML models, and collaborate with teams to address business needs through advanced machine learning techniques.

The Clinical Research Associate II will monitor clinical trials, train site staff, ensure compliance with GCP, and report study data.

Responsible for lifecycle management of drug products, preparing regulatory submissions, and ensuring compliance with regulations. Works with cross-functional teams and mentors junior staff.

Oversee client model management, enhance clinical trial innovation projects, and strengthen connections with various stakeholders in clinical operations.

The Senior Clinical Research Associate manages site monitoring and relationships for clinical trials, ensuring compliance and patient safety according to GCP and regulations.

The Senior Clinical Trial Manager oversees operational aspects of clinical trials from start-up to database lock, ensuring compliance with GCP and SOPs, managing vendors, and coordinating trial activities and communications with stakeholders.

The Scientist III supports laboratory operations by maintaining LC-MS instruments, troubleshooting issues, and performing LC and LC-MS analysis for investigational compounds.

This role involves executing chromatographic purification, characterizing purified samples, conducting lab experiments, and documenting results while collaborating with various teams.

The Clinical Research Associate is responsible for site management, monitoring clinical studies, ensuring compliance with regulations, and supporting site staff in study-related matters.