Clinical Trials Coordinator & Research Specialist

OhioHealth; Columbus (OH); Vor Ort; USD 75.000 - 115.000; Vollzeit

Zusammenfassung

OhioHealth in Columbus, OH is seeking a Clinical Consultant Research to work with the Principal Investigator to coordinate assigned clinical studies according to GCP and federal regulations.

You will recruit and screen participants, obtain informed consent, collect data, and support study visits, while maintaining study documentation and communicating with sponsors. This role emphasizes protocol adherence and data integrity in a collaborative, high-reliability health system.

Qualifikationen

• Bachelor's Degree required.
• Strong verbal and written communication and customer service skills.
• Thorough knowledge of EMR and Microsoft systems.
• Clinical Research Coordinator Certification and/or equivalent preferred.
• Experience in medical environment preferred.

Aufgaben

• Coordinate approved clinical studies under the Principal Investigator (PI).
• Assist with recruitment and enrollment procedures and screen participants.
• Ensure protocol adherence and accurate data collection and entry.
• Prepare study documents for archiving and maintain source documentation.
• Attend study-related meetings and communicate with sponsor representatives.

Kenntnisse

Communication skills

Problem solving

Time management

Customer service skills

Multitasking

EMR knowledge

Microsoft Office

Ausbildung

Bachelor's Degree

Tools

EMR

Microsoft Office

Jobbeschreibung

OhioHealth in Columbus, OH is seeking a Clinical Consultant Research to work with the Principal Investigator to coordinate assigned clinical studies according to GCP and federal regulations.

You will recruit and screen participants, obtain informed consent, collect data, and support study visits, while maintaining study documentation and communicating with sponsors. This role emphasizes protocol adherence and data integrity in a collaborative, high-reliability health system.