Senior Associate Study Manager

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

Key Responsibilities

Assist in study planning, vendor management, and coordination of study implementation plans

Prepare, write, and review study-related documents and ensure quality checks on protocols and consent forms

Coordinate site start-up activities and manage study budgets and timelines

Required Qualifications

Knowledgeable in ICH, GCP, FDA regulations, and international regulatory standards

Experienced in interactions with external vendors and site selection criteria development

Well-versed in the drug development process and related procedures

Educated with a Master's degree, or a Bachelor's / RN with 3+ years of experience, or an Associate's with 6+ years, or a High School diploma with 10+ years in a life sciences or medically related field