A company is looking for a Principal Clinical Research Associate (CRA) to oversee and manage clinical trial sites remotely.Key ResponsibilitiesLead site management activities, ensuring compliance with study protocols and regulatory guidelinesServe as the primary point of contact for clinical sites, addressing queries and resolving issuesMentor and provide guidance to CRAs, supporting their professional development and best practicesRequired QualificationsBachelor's degree in life sciences, nursing, pharmacy, or a related field; advanced degree preferredExtensive experience as a Clinical Research Associate in the pharmaceutical, biotech, or CRO industryIn-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processesStrong leadership and mentoring skills to effectively manage and motivate CRAs and site staffProactive approach to managing site performance and resolving issues