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Launching a Career as a Clinical Research Project Manager | Clinical Trials Training Clinical research project manager training is essential for professionals responsible for planning, oversight, and delivery of complex clinical trials. This lesson, Launching Your Career as a Clinical Project Manager, explains how project managers operate within regulated clinical research environments to ensure timelines, quality, and compliance are met across global studies. Delivered within the Advanced Clinical Research Project Manager Certification (ACPMC) pathway, this session outlines the core responsibilities of clinical project managers, including protocol planning, cross-functional coordination, risk management, budget and milestone tracking, vendor oversight, and inspection readiness. Learners gain practical insight into how project leadership supports compliant execution across Phase I–IV clinical trials. The lesson connects clinical research training to real-world trial operations, highlighting how project managers collaborate with sponsors, CROs, CRAs, CRCs, pharmacovigilance teams, and investigators to maintain data integrity, subject safety, and regulatory alignment. Emphasis is placed on ICH GCP–aligned governance, documentation standards, issue escalation, and performance oversight across multi-site and global trials. This content is part of CCRPS’s triple accredited clinical research training ecosystem, designed to reflect how clinical research project managers function in active trial settings rather than theoretical models. The ACPMC pathway includes role-specific coursework with extensive lessons, live weekly webinars, applied case studies, operational toolkits, MCQs, and simulation-based learning aligned with global clinical research standards. This lesson is intended for experienced CRCs, CRAs, clinical operations professionals, and life science graduates seeking structured preparation for leadership roles in clinical trials management and project oversight. This lesson is part of CCRPS’s role specific clinical research certification pathways, designed to match the day to day responsibilities of professionals working as CRCs, CRAs, pharmacovigilance specialists, project managers, and investigators across global trials. Learn more: https://ccrps.org Explore programs: https://app.ccrps.org Call advising: +1 801 515 4867 Educational Disclaimer: ------------------------------------- The content provided on this channel is intended for educational and informational purposes only. CCRPS does not provide medical advice, clinical treatment recommendations, legal guidance, or professional services through this content. All information shared is based on general principles of clinical research, regulatory standards, and industry practices and should not be considered a substitute for professional judgment, institutional policies, or regulatory requirements. Viewers are encouraged to consult qualified professionals, official guidelines, and regulatory authorities before applying any information in clinical, research, or professional settings. CCRPS assumes no responsibility for actions taken based on the content presented in these videos.