Descripción de la oferta
Lead CRALas cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.We are seeking an experienced Lead CRA to support Phase 2–3 clinical trials across liver and cardiometabolic indications, including MASH/NASH, obesity, and related metabolic disorders.This role will play a critical part in ensuring high-quality site execution, regulatory compliance, and data integrity across complex, multi-center studies. The ideal candidate will bring strong therapeutic expertise alongside leadership capability within a dynamic clinical environment.Key ResponsibilitiesOversee clinical trial site activities to ensure strict adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conduct routine and ad hoc site visits to evaluate performance, identify risks, resolve operational challenges, and support successful study delivery.Partner closely with cross-functional teams to ensure accurate, timely data capture and reporting throughout the study lifecycle.Provide training, mentorship, and ongoing guidance to site personnel and fellow CRAs to uphold high standards of trial conduct and compliance. xiphtebDevelop and maintain strong, collaborative relationships with investigators, site staff, and key stakeholders to promote efficient and compliant trial execution.Required Qualifications6–10+ years of CRA experience with at least 2+ years operating at a senior or Lead CRA levelDemonstrated experience in liver disease, MASH/NASH, obesity, diabetes, or cardiometabolic clinical trialsExperience managing complex endpoints such as liver biopsy coordination, imaging (MRI-PDFF, FibroScan), and metabolic biomarkersStrong knowledge of ICH-GCP and regulatory requirementsExperience working in high-enrolling academic and community sitesWillingness to travel as required
