Sleep Medicine Clinical Research Coordinator – Dublin

Vituity; Dublin (OH); On-site; USD 41,000 - 52,000; Full time

Benefits offered by this job

Health plan

Dental & Vision

401(k) match

PTO

Sabbatical

Student loan discounts

Career development

Wellness program

Commuter benefits

Travel assistance

EAP

Job summary

Vituity in Dublin, OH, seeks a Clinical Research Coordinator to coordinate sleep medicine trials, recruit participants, obtain informed consent, and support data collection and regulatory activities. The role emphasizes meticulous documentation, adherence to GCP and HIPAA, and collaboration with investigators and sponsors.

The coordinator will perform blood draws, vitals, ECGs, and use EDC systems, while ensuring data integrity and compliance across study visits and regulatory expectations.

Qualifications

• Bachelor’s degree in a healthcare-related field is required.
• CPR and Phlebotomy certification are required.
• GCP knowledge and FDA human subjects research regulations are required.
• 1+ years of clinical research coordination experience preferred.
• Experience with sleep medicine, pulmonary, or neurology trials preferred.
• Familiarity with EDC systems and IRB portals preferred.

Responsibilities

• Coordinate study visits from screening through closeout.
• Recruit and screen participants and obtain informed consent.
• Support regulatory submissions and adverse event reporting.
• Collect and record study data and maintain documentation.
• Perform procedures like blood draws, vitals, and ECGs.
• Enter data into sponsor EDC and resolve data queries.
• Ensure compliance with GCP, HIPAA, and regulations.

Skills

CPR Certification

Phlebotomy Certification

GCP knowledge

EDC systems

IRB submissions

Clinical data collection

Documentation accuracy

HIPAA compliance

Strong communication

Independent work

Education

Bachelor's degree in healthcare-related field

Tools

EDC systems

Clinical trial management software

IRB submission portals

Job description

Vituity in Dublin, OH, seeks a Clinical Research Coordinator to coordinate sleep medicine trials, recruit participants, obtain informed consent, and support data collection and regulatory activities. The role emphasizes meticulous documentation, adherence to GCP and HIPAA, and collaboration with investigators and sponsors.

The coordinator will perform blood draws, vitals, ECGs, and use EDC systems, while ensuring data integrity and compliance across study visits and regulatory expectations.