Clinical Research Coordinator: Study Ops & Patient Engagement

OhioHealth Corporation; Columbus (OH); Vor Ort; USD 60.000 - 85.000; Vollzeit

Zusammenfassung

OhioHealth Corporation is seeking a Clinical Consultant Research who will coordinate assigned clinical studies in line with GCP and federal regulations. The role involves recruiting and screening participants, obtaining informed consent, educating participants on study requirements, and collecting data.

You will assist in study planning, ensure accurate data recording, and support monitor visits. Candidates should be able to work under supervision across diverse studies, maintaining compliant

Qualifikationen

• Coordinating clinical research studies in accordance with GCP guidelines and federal regulations.
• Recruiting and screening participants, obtaining informed consent, and educating participants about study requirements.
• Accurate data collection and completion of case report forms.

Aufgaben

• Assist with study planning and coordination under PI supervision.
• Oversee enrollment of participants and monitor visits as directed by the PI.
• Maintain study records and source documentation with timeliness and accuracy.
• Prepare documents for archiving according to timelines and closeout activities.
• Communicate with sponsors, investigators, and clinical teams to review patient status and study procedures.

Kenntnisse

Clinical research

Good Clinical Practice

Informed consent

Data collection

Communication

Jobbeschreibung

OhioHealth Corporation is seeking a Clinical Consultant Research who will coordinate assigned clinical studies in line with GCP and federal regulations. The role involves recruiting and screening participants, obtaining informed consent, educating participants on study requirements, and collecting data.

You will assist in study planning, ensure accurate data recording, and support monitor visits. Candidates should be able to work under supervision across diverse studies, maintaining compliant