Senior Clinical Research Coordinator Full Time - 1st Shift

daytonchildrens; Dayton (OH); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

Dayton Children's is seeking a Senior Clinical Research Coordinator in the Neurology department at the Main Campus to lead clinical research activities according to ICH/GCP guidelines.

The role involves site feasibility, patient screening, enrollment, conducting study visits, and ensuring high-quality data and source documents. Shift is 8:00AM–4:30PM, Monday–Friday, with full-time hours.

Qualifications

• Bachelor's degree in health sciences or a related field required.
• Strong organizational skills, proficiency in EDC systems, and ability to work independently.
• Preferred 3+ years of experience in clinical research.

Responsabilités

• Site feasibility and study preparation.
• Screening and recruitment of patients and enrollment.
• Conducting study visits and ensuring data quality.

Connaissances

Strong organizational skills

Independent work

Formation

Bachelor's degree in health sciences

Outils

EDC systems

Description du poste

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