A company is looking for a Clinical Scientist Associate Director, Late Development Obesity.
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 consistency and clarity
Provide input into data management plans and oversee data review and analysis for clinical trials
Required Qualifications
Doctorate degree with 3 years, or Master's degree with 5 years, or Bachelor's degree with 7 years, or Associate's degree with 12 years, or High school diploma / GED with 14 years of clinical development experience
3 years of pharmaceutical clinical drug development experience preferred
Experience contributing to clinical trial process improvements within a therapeutic area
Knowledge of Good Clinical Practice standards and applicable regulatory requirements
Experience in clinical data analysis and supporting regulatory submission documents
mid
4/3/2026
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