A company is looking for a Senior Associate Study Manager.
Key Responsibilities
Support the execution and monitoring of clinical studies and trial deliverables
Participate in study planning, vendor management, and coordination of study activities
Prepare 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, or Associate's with 6+ years, or High School diploma with 10+ years in a life sciences or medically related field
Knowledge of ICH, GCP, and FDA regulations
Experience in interactions with external vendors
Skilled in project planning and management of study deliverables
Well-versed in the drug development process and related procedures
Senior Associate • West Palm Beach, Florida, United States