Senior Clinical Trial Coordinator

Job Description

Qualifications

• •BA / BS or equivalent experience in scientific or healthcare disciplines
• •Minimum of two years of experience in clinical research, preferably with medical device or pharmaceutical trials
• •Proficiency in MS Windows-based applications
• •Working knowledge of ICH Good Clinical Practice guidelines
• •Valid driver's license and ability to travel domestically up to 10%

Benefits

Responsibilities

• •Manage the Trial Master File (TMF) and Investigator Site File (ISF) for clinical studies
• •Track and review study-specific documents and manage device accountability
• •Oversee study budgets, payments, and maintain audit readiness of study documentation