Senior Clinical Research Coordinator Full Time - 1st Shift

Myana; Dayton (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

Myana seeks a Senior Clinical Research Coordinator for Dayton Children's - Main Campus in the Neurology department. The role involves leading clinical research activities under supervision, ensuring ICH/GCP compliance, and maintaining high-quality study standards.

Responsibilities include patient screening, enrollment, site feasibility, conducting visits, and meticulous data handling with CRFs and source documents, all while safeguarding participant well-being.

Qualifications

• Bachelor's degree in health sciences or a related field.
• Strong organizational skills and ability to work independently.
• Experience with Electronic Data Capture (EDC) systems preferred.

Responsibilities

• Lead site feasibility and study preparation activities.
• Screen and recruit patients; oversee enrollment and visits.
• Complete case report forms accurately and maintain source documents.
• Monitor study quality and ensure regulatory compliance (ICH/GCP).

Skills

Strong organizational skills

Ability to work independently

EDC proficiency

Education

Bachelor's degree in health sciences or related field

Tools

Electronic Data Capture (EDC) proficiency

Job description

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