Principal Clinical Research Associate

Job Summary

A company is looking for a Principal Clinical Research Associate (CRA) to oversee and manage clinical trial sites remotely.

Key Responsibilities

• Lead site management activities, ensuring compliance with study protocols and regulatory guidelines
• Serve as the primary point of contact for clinical sites, addressing queries and resolving issues
• Mentor and provide guidance to CRAs, supporting their professional development and best practices

Required Qualifications

• Bachelor's degree in life sciences, nursing, pharmacy, or a related field; advanced degree preferred
• Extensive experience as a Clinical Research Associate in the pharmaceutical, biotech, or CRO industry
• In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes
• Strong leadership and mentoring skills to effectively manage and motivate CRAs and site staff
• Proactive approach to managing site performance and resolving issues