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

fessional development and best practices Required Qualifications Bachelor&#39;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

Principal Clinical Research Associate

Behavioral Health Market Context

Job Description