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 clinical trial management staff in executing and monitoring clinical studies and trial deliverables
• Participate in study planning, vendor management, and preparation of study-related documents
• Coordinate site start-up activities and manage study budgets and timelines

Required Qualifications

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