Senior Associate Study Manager

Job Summary

A company is looking for a Senior Associate Study Manager to support the execution and monitoring of clinical studies.

Key Responsibilities

• Support execution and monitoring of clinical studies and trial deliverables
• Participate in study planning, vendor management, and coordination of study implementation plans
• Prepare, write, and review study-related documents and manage study budgets and timelines

Required Qualifications

• Master's degree or Bachelor's/RN with 3+ years of experience, Associate's with 6+ years, or High School diploma with 10+ years in a life sciences or medically related field
• Knowledge of ICH, GCP, FDA regulations, and international regulatory standards
• Experience in vendor interactions and site-selection criteria development
• Proficient in project planning, study deliverables, budgets, and timelines
• Well-versed in the drug development process and related procedures