Lead Site/Study Coordinator - Remote

Overview

The Lead Site/Study Coordinator supports clinical trial conduct at medical institutions while ensuring compliance with protocols and regulations.

In Short

• Acts as a liaison between medical institutions and sponsors/CROs.
• Facilitates study feasibility assessments and patient recruitment.
• Conducts quality checks for compliance with protocols.
• Trains site staff on clinical research best practices.
• Ensures accurate data entry into EDC systems.
• Supports contract and budget negotiations.
• Maintains study documentation for audits and inspections.
• Identifies areas for improvement in study processes.
• Participates in the development of training programs.
• Maintains licensure and certifications applicable to the role.

Requirements

• Associate Degree (Nursing preferred) and 5 years of relevant experience.
• Current Good Clinical Practice (GCP) certification.
• International Air Transport Association (IATA) certification.
• Basic Cardiopulmonary Resuscitation (CPR) certification.
• Phlebotomy certification (if not part of active professional licensure).
• Active Certification in Clinical Research by ACRP or SOCRA.
• Proficiency in patient assessments and multi-therapeutic protocol design.
• Strong communication and organizational skills.
• Proficient in Microsoft Office and EDC/EMR systems.
• Ability to work in a fast-paced environment with multiple tasks.

Benefits

• Opportunity to work in a growing field of clinical research.
• Engagement in innovative practices and teamwork.
• Access to training and professional development.
• Flexible working hours with remote work options.
• Supportive work environment with a focus on quality.