Clinical Scientist Associate Director

Job Summary

Supporting the design and execution of global cardiovascular trials, the full-time remote Clinical Scientist Associate Director will oversee protocol development, medical monitoring, and clinical data review to ensure high-quality data for regulatory submissions and scientific dissemination.

Key responsibilities

• Support the design, start-up, and execution of global cardiovascular trials, ensuring adherence to protocols and regulatory requirements
• Contribute to the development of clinical protocols, statistical analysis plans, and regulatory documents with a focus on cardiovascular endpoints
• Collaborate with cross-functional teams to support endpoint strategy and safety monitoring while conducting ongoing clinical data review

Required qualifications

• Doctorate degree and 3 years of clinical development experience, or Master's degree and 5 years, or Bachelor's degree and 7 years, or Associate's degree and 12 years, or High school diploma/GED and 14 years of clinical development experience
• 3 years of pharmaceutical clinical drug development experience, particularly in late-stage global clinical trials
• Experience in cardiovascular medicine and/or outcomes trials, with a preference for large event-driven studies
• Knowledge of Good Clinical Practice standards and applicable regulatory requirements
• Experience contributing to regulatory submission documents and supporting clinical regulatory responses