Clinical Research Coordinator - Remote

Overview

Vitalief is a leading site solutions partner focused on improving the value and contribution of clinical trial sites across the drug development lifecycle. With deep expertise in Consulting (strategic and operational) and Functional Service Provider (FSP) services, we provide fully integrated solutions that streamline clinical trials, improve patient outcomes, and drive value for Sponsors, CROs, and sites.

In Short

• Seeking a motivated Clinical Research Coordinator for decentralized clinical trials.
• Contribute to advancing scientific discoveries impacting patients' lives.
• Prioritize personal and professional growth in a PEOPLE FIRST culture.
• Encourage innovation with a seat at the table for all employees.
• Enjoy 20 PTO days plus 9 paid holidays annually.
• Receive benefits including life insurance, disability coverage, and 401K.
• Work remotely with standard business hours in PT.
• Accountable for successful execution of clinical trials.
• Coordinate and execute all aspects of clinical research studies.
• Communicate effectively with trial participants and team members.

Requirements

• Bachelor's Degree preferred; GCP certification required.
• Minimum 2 years experience as a Clinical Research Coordinator.
• Experience in patient recruiting, regulatory compliance, and data management.
• Behavioral Health experience is a plus.
• Exceptional communication and time management skills.
• Strong organizational skills with attention to detail.
• Proficient in Microsoft Office and EHR systems.
• Ability to troubleshoot and adapt to changing priorities.

Benefits

• 20 PTO days plus 9 paid holidays annually.
• Company paid life insurance and disability coverage.
• 401K retirement program.
• Robust healthcare plans to choose from.
• People-first culture prioritizing growth and innovation.