Clinical Research Associate (CRA) - Remote

Overview

This is an open application for Clinical Research Associates with at least 2 years of independent monitoring experience for future needs. There is currently no active opening for this position yet.

In Short

• Independently manage all aspects of monitoring for assigned clinical trials.
• Ensure compliance with protocols, GCP, ICH, SOPs, and regulatory requirements.
• Build strong relationships with sites and act as a primary contact.
• Identify and resolve site issues to maintain trial integrity.
• Mentor junior CRAs and share best practices.
• Travel throughout the United States.
• Proactively detect issues and provide solutions.
• Support a collaborative and experienced team.
• Contribute to the success of small-medium biopharmaceutical companies.
• Work in a caring and team-oriented environment.

Requirements

• At least 2 years of independent monitoring experience.
• Strong knowledge of clinical trial protocols and GCP.
• Excellent communication and interpersonal skills.
• Ability to travel as required.
• Experience in mentoring junior team members.

Benefits

• Be part of a dedicated team helping biopharmaceutical companies.
• Opportunity to grow and develop professionally.
• Work in a supportive and collaborative environment.
• Contribute to life-changing therapies for patients.