Senior Clinical Research Coordinator - Full Time - 1st Shift

Myana; Dayton (OH); Presencial; USD 65.000 - 90.000; Tempo integral

Resumo da vaga

Dayton Children's - Main Campus in Dayton, OH seeks a Senior Clinical Research Coordinator in Neurology to lead clinical studies under supervision, ensuring high-quality conduct per ICH and GCP guidelines.

Responsibilities include feasibility, patient screening and enrollment, conducting visits, data collection, and maintaining source documents to ensure site quality and participant safety.

Qualificações

• Bachelor's degree in health sciences or related field.
• Strong organizational skills and ability to work independently; proficiency in EDC systems.

Responsabilidades

• Site feasibility and study preparation.
• Patient screening, recruitment and enrollment.
• Conducting study visits per protocol.
• Completing and ensuring quality of case report forms.
• Maintaining source documents and trial records.
• Ensuring site quality and regulatory compliance.
• Adhere to ICH and GCP guidelines to protect participants.

Conhecimentos

Organizational skills

EDC proficiency

Independent work

Formação

Bachelor's degree in health sciences or related field

Ferramentas

EDC systems

Descrição da vaga

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