Senior Clinical Trial Coordinator
Behavioral Health Market Context
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Job Description
ientific 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%
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%
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
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