• Lead the Clinical Data Management function at RayzeBio, providing strategic and operational oversight across the clinical portfolio. • Serve as the Data Management lead for a high-priority clinical development program, maintaining hands-on involvement in study execution, data review, issue resolution, and risk management. • Provide leadership for NDA/BLA submission activities, including submission readiness, data standards compliance, and regulatory inspection preparedness. • Partner cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, Safety, and Regulatory Affairs to support study execution and data quality objectives. • Oversee CROs and vendors, ensuring quality, compliance, accountability, and adherence to timelines and deliverables. • Lead ongoing cross-functional data review activities and oversee the development of key data management documentation, including Data Management Plans, edit checks, validation specifications, reconciliation plans, and data transfer agreements. • Develop and implement scalable data management processes, standards, governance, and SOPs to support operational excellence and organizational growth. • Manage competing priorities across multiple studies while proactively identifying operational risks and mitigation strategies. • Build, develop, and expand the Clinical Data Management team, and foster a collaborative and high-performing team environment. • Willing to travel approximately 10% of the time. Evening and weekend work will be involved.

• Build, grow, and lead a high-performing clinical admissions team—recruiting, hiring, and onboarding Clinical Admissions Managers, Leads, Therapists, and Associates to keep pace with admissions growth • Provide individual and group supervision to a team of masters-level clinicians, promoting growth and development • Set clear goals and expectations, monitor performance against metrics, and performance-manage the team through coaching, feedback, and accountability • Develop and coach managers and leads, strengthening their ability to lead, develop, and performance-manage their own teams • Foster a culture of engagement, retention, and sustainability across a remote team working in an emotionally demanding environment • Assign treatment team members and group schedules while informing staff of new admissions • Oversee intake and assessments of prospective clients for national virtual intensive outpatient programming • Lead and support the team of managers, therapists, and associates in converting prospective clients to care—confirming clinical fit and, when clients are appropriate, getting them scheduled into programming as quickly as possible • Ensure completion of HIPAA-compliant virtual biopsychosocial assessments for adolescents, young adults, and adults with various mental health concerns • Determine appropriateness and fit for the virtual intensive outpatient program (IOP) level of care, and equip the team to make consistent, accurate fit decisions • Drive speed to admit by minimizing the time from assessment to a scheduled start so clients can begin care without delay • Construct provisional mental health diagnoses utilizing DSM-5-TR criteria • Identify and connect with appropriate staff when crisis intervention, a safety assessment, or a higher level of care (HLOC) is needed during the intake process • Model and coach personable, competent communication that builds rapport with clients in a compassionate, inclusive, and professional manner • Ensure programming information is presented thoroughly and supportively to help clients gain access to care • Complete monthly chart audits to ensure compliance and quality assurance • Document client information in accordance with regulatory standards using the electronic medical record • Lead change management initiatives, driving the smooth rollout and adoption of new processes, workflows, and policies across the admissions team • Build, refine, and scale admissions processes that improve speed, quality, consistency, and conversion as the team and client volume grow • Monitor team and funnel performance, identify bottlenecks, and implement improvements that raise both clinical quality and operational efficiency • Partner across departments to ensure clinically appropriate admissions and effective team performance, aligning closely with your fellow Director of Clinical Admissions • Collaborate with Clinical Leadership, Admissions, Compliance, Revenue Cycle Management, and Utilization Review to identify opportunities for growth while developing, enhancing, and delivering policies and procedures that improve the quality of the client experience and increase the efficacy of the admission process • Ensure the completion of projects and initiatives that better support clients in obtaining access to care • Perform other duties as assigned

Role Description GovCIO is currently hiring a part-time Radiology/Nuclear Medicine Subject Matter Expert (SME) to support the Health Services Portfolio Technical Management and Strategic Solutioning Support (HTMS) program within the Department of Veterans Affairs (VA) Office of Information and Technology (OIT). This role is a fully remote position within the United States. Core office hours are 8am – 5pm ET; this position is part-time, 29 hours per week. - Serves as the principal advisor and subject matter expert for Radiology and Nuclear Medicine Health Level Seven (HL7), Valid Data Length (VDL) for primary and secondary diagnostic codes for business rules and processes, workflow standardization, governance, stakeholder engagement, and operational support. - Provides strategic guidance to leadership, program offices, and technical teams to ensure consistent implementation, sustainment, and modernization of Radiology and Nuclear Medicine services across the enterprise. - Provides expert consultation on Radiology and Nuclear Medicine operational workflows, policies, procedures, SNOW tickets, and best practices. - Supports enterprise-wide Radiology and Nuclear Medicine standardization initiatives. - Assists in evaluating operational impacts of proposed changes, enhancements, and regulatory requirements. - Identifies opportunities for process improvement and workflow optimization. - Provides operational analysis and business impact assessments for incidents affecting Radiology and Nuclear Medicine services. - Assists in prioritizing issues based on clinical impact, patient safety considerations, and organizational risk. - Coordinates with stakeholders to facilitate timely resolution of operational concerns. - Provides issue analysis and recommended steps and preventative measures on problematic SNOW tickets. Qualifications - Master’s degree in computer science, electronics engineering or other engineering or technical discipline is required, plus 10 years of experience. 10 years of additional relevant experience may be substituted for education. - Extensive experience supporting Radiology and/or Nuclear Medicine operations within a healthcare environment. - Extensive experience in troubleshooting Rad and nuclear medicine SNOW tickets and domain knowledge of Radiology packages. - Demonstrated knowledge of clinical workflows, imaging operations, and healthcare business processes. - Ability to analyze complex operational issues and provide strategic recommendations. - Experience developing policies, procedures, governance documents, and operational guidance. - Veterans’ Health Information Systems and Technology Architecture (VistA). - Proficient with MS Office (Word, Excel, PowerPoint, Visio). - Proficient with MS SharePoint and MS Teams. Requirements - Experience supporting the U.S. Department of Veterans Affairs (VA) healthcare environment. - Knowledge of VA Radiology and Nuclear Medicine workflows and enterprise initiatives. - Familiarity with accreditation standards, compliance requirements, and healthcare quality improvement initiatives. - Prior software developer and release management experience. - Understand software such as GitHub and FORUM. - Ability to work in a fast-paced, collaborative environment. - Excellent prioritization and time management skills. - Excellent attention to detail and ability to meet deadlines and stay organized. Clearance Required - Ability to obtain and maintain a VA Public Trust clearance. Posted Salary Range USD $90,480.00 - USD $95,004.00 /Yr.

Role Description The Medical Monitor / Study Physician is responsible for providing medical oversight of clinical trials, ensuring patient safety, protocol compliance, and high quality study conduct. The role involves close collaboration with clinical teams, investigators, and sponsors to support successful study execution. As part of our SRS FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area. Key Responsibilities - Provide medical oversight for clinical trials, ensuring patient safety and protocol adherence - Review patient eligibility and ongoing safety data within studies - Support development and review of study protocols and clinical documents - Act as medical point of contact for investigators and clinical teams - Contribute medical expertise to study conduct, issue resolution, and decision making Qualifications - Medical Doctor degree - Strong experience in clinical trials, ideally in a Study Physician or Medical Monitor role - Background within neurology, ideally with experience in pediatric neurology or related indications - Good understanding of GCP and clinical trial processes - Ability to work independently and collaborate in cross functional teams - Strong written and verbal communication skills in English Benefits - Opportunities for personal and professional growth in a rewarding environment - A team that values collaboration, quality, and making a difference in the lives of patients - Core values of Trust, Quality, Passion, Flexibility, and Sustainability guiding decisions and shaping culture Company Description Our journey began over 30 years ago in Sweden, in the city of Lund. As a full service global CRO, we build solution driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.