{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/bgr-remote/"},"x-facet":{"type":"city","slug":"bgr-remote","display":"Bgr-remote","count":4},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_98234501-3d0"},"title":"Clinical Trial Manager II or Senior","description":"<p>Syneos Health is seeking a Clinical Trial Manager II or Senior to join their team. The successful candidate will be responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Responsible for site management oversight, clinical monitoring, and central monitoring deliverables</li>\n<li>Oversees site interactions post-activation through site closeout</li>\n<li>May be responsible for identification of critical data and process, protocol execution risks, and risk mitigations</li>\n<li>Reviews the study scope of work, budget, and protocol content</li>\n<li>Uses prior clinical experience, operational data, metrics, and reports to identify risks to clinical trial management deliverables</li>\n<li>Escalates to the project manager any risks to clinical trial management deliverables</li>\n<li>Employs strategic thinking and problem-solving skills to propose and implement risk mitigations</li>\n<li>Participates and presents in key meetings</li>\n<li>Serves as an escalation point for communications with investigator site staff</li>\n<li>Collaborates with other functional leaders to coordinate delivery handoffs and meet expected study milestones</li>\n<li>Responsible for development and ongoing maintenance of clinical study tools and templates</li>\n<li>Coordinates initial and ongoing training to the study team</li>\n<li>Oversees resourcing allocations for CRAs and Central Monitors, site assignments, and study team members&#39; conduct</li>\n<li>Ensures quality of the clinical monitoring, central monitoring, and site management deliverables</li>\n<li>Reviews the project oversight dashboards and other clinical trial systems</li>\n<li>Understands the monitoring strategy required for the study and participates in the development of the study risk assessment plan</li>\n<li>Reviews the content and quality of site and central monitoring documentation</li>\n<li>Interacts with the client and other functional departments related to clinical monitoring, central monitoring, and site management activities and deliverables</li>\n<li>Demonstrates understanding of other functions&#39; roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP, and country regulations</li>\n<li>Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance</li>\n<li>Provides feedback to line managers on staff performance</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Demonstrated ability to lead and align teams in the achievement of project milestones</li>\n<li>Demonstrated capability of working in an international environment</li>\n<li>Demonstrated expertise in site management and monitoring</li>\n<li>Preferred experience with risk-based monitoring</li>\n<li>Demonstrates understanding of clinical 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