Clinical Scientist Associate Director

Job Summary

Supporting oncology late-phase clinical development, the full-time remote Clinical Scientist Associate Director will manage protocol development, study start-up, and data review to ensure high-quality clinical data for decision-making.

Key responsibilities

• Support the setup and execution of late-phase clinical trials with a focus on data quality
• Assist in authoring clinical protocols and regulatory documents, ensuring clarity and consistency
• Provide oversight for clinical trial data review and analysis for internal decision-making and regulatory submissions

Required qualifications

• Doctorate degree with 3 years, Master's degree with 5 years, Bachelor's degree with 7 years, Associate's degree with 12 years, or High school diploma/GED with 14 years of clinical development experience
• 3 years of experience in a pharmaceutical industry setting, preferably in oncology
• Experience in contributing to clinical trial process improvements
• Strong understanding of Good Clinical Practice standards and regulatory requirements
• Experience with clinical data analysis tools and contributing to regulatory submission documents