Central Study Coordinator - Remote

Overview

The Central Study Coordinator (CSC) position combines clinical research and project management skills into a singular role that delivers a strong customer experience for both patients and sites.

In Short

• Manage study work for each assigned site as delegated by the PI.
• Build strong rapport with sites, participants, CRAs, and sponsor contacts.
• Host regular calls with each assigned PI and present on key elements of the study.
• Facilitate communication between study site, CRA, and sponsor.
• Perform the Informed Consent process with study participants virtually.
• Schedule, prepare for, and facilitate participant visits in accordance with the study protocol.
• Enter data and resolve queries in EDC and other portals.
• Ensure all study trackers and systems are up to date daily.
• Support site compliance with subject safety reporting.
• Additional duties and responsibilities may be assigned as needed.

Requirements

• At least 3 years of relevant clinical research experience.
• Proficient with Microsoft Office applications.
• Strong communication customer service abilities.
• High attention to detail.
• Ability to work effectively in a remote environment.
• Proper home office set-up including a private space for participant communication.

Benefits

• PTO/vacation days, sick days, holidays.
• 100% paid medical, dental, and vision Insurance.
• HSA plan.
• Short-term disability, long-term disability, and life Insurance.
• 401k retirement plan.