What are the responsibilities and job description for the Senior Clinical Research Coordinator Full Time - 1st Shift position at Dayton Children's Hospital?
Facility
Dayton Children's - Main Campus
Department
Neurology
Schedule
Full time
Hours
40
Job Details
The Senior Clinical Research Coordinator will perform clinical research activities under minimal direction of the Clinical Research Supervisor/Manager and a Principal Investigator (PI), while adhering to International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines. The Coordinator will play a lead role in assigned studies and will be critical to ensuring all studies are conducted to a high standard of quality. The Coordinator will perform tasks including, but not limited to, site feasibility and preparation, patient screening and recruitment, patient enrollment, conducting study visits, completing and ensuring the quality of case report forms, maintaining source documents, and ensuring site quality.
All clinical research activities must be conducted in accordance with applicable federal and state regulations. Most importantly, the Senior Clinical Research Coordinator will ensure the safety and well-being of all study participants throughout all study activities.
Required Qualifications
Bachelor’s degree in health sciences or a related field
Strong organizational skills, proficiency in Electronic Data Capture (EDC) systems, and ability to work independently.
Preferred Qualifications
3 years of experience in clinical research
Department Specific Job Details
Shift: 8:00AM - 4:30PM, Monday - Friday
Dayton Children's - Main Campus
Department
Neurology
Schedule
Full time
Hours
40
Job Details
The Senior Clinical Research Coordinator will perform clinical research activities under minimal direction of the Clinical Research Supervisor/Manager and a Principal Investigator (PI), while adhering to International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines. The Coordinator will play a lead role in assigned studies and will be critical to ensuring all studies are conducted to a high standard of quality. The Coordinator will perform tasks including, but not limited to, site feasibility and preparation, patient screening and recruitment, patient enrollment, conducting study visits, completing and ensuring the quality of case report forms, maintaining source documents, and ensuring site quality.
All clinical research activities must be conducted in accordance with applicable federal and state regulations. Most importantly, the Senior Clinical Research Coordinator will ensure the safety and well-being of all study participants throughout all study activities.
Required Qualifications
Bachelor’s degree in health sciences or a related field
Strong organizational skills, proficiency in Electronic Data Capture (EDC) systems, and ability to work independently.
Preferred Qualifications
3 years of experience in clinical research
Department Specific Job Details
Shift: 8:00AM - 4:30PM, Monday - Friday