Maryland Licensed Clinical Research Monitor
A company is looking for a Clinical Research Monitor who will lead compliance monitoring of clinical trials. Key Responsibilities Manage site and study progress by tracking regulatory submissions and data query resolution Conduct risk assessments and develop monitoring plans based on findings Ensure compliance with regulatory requirements and assist in training research staff Required Qualifications Bachelor's Degree in a related field Minimum 5 years of experience with clinical trials or medical research Thorough knowledge of ICH GCP and FDA guidelines Experience using Electronic Data Capturing (EDC) systems Additional education may substitute for required experience as permitted by the equivalency formula
A company is looking for a Clinical Research Monitor who will lead compliance monitoring of clinical trials.
Key Responsibilities
Manage site and study progress by tracking regulatory submissions and data query resolution
Conduct risk assessments and develop monitoring plans based on findings
Ensure compliance with regulatory requirements and assist in training research staff
Required Qualifications
Bachelor's Degree in a related field
Minimum 5 years of experience with clinical trials or medical research
Thorough knowledge of ICH GCP and FDA guidelines
Experience using Electronic Data Capturing (EDC) systems
Additional education may substitute for required experience as permitted by the equivalency formula
