• Lead and manage global Phase I virology clinical trials from study start-up through closeout with minimal supervision • Drive overall study execution, timelines, deliverables, risks, budgets, and operational performance • Provide oversight and accountability for CROs, vendors, and cross-functional partners to ensure high-quality study execution • Build strong collaborative relationships with Clinical Operations, Data Management, Regulatory, Medical, Clinical Supply, Biometrics, and other stakeholders • Lead study team meetings by establishing clear agendas, facilitating productive discussions, documenting key decisions, and ensuring timely completion of action items • Proactively identify operational risks, develop mitigation strategies, and drive issue resolution before timelines or quality are impacted • Guide study teams through key transitions across the clinical trial lifecycle while ensuring seamless operational execution • Maintain oversight of study documentation, trial metrics, operational deliverables, and inspection readiness activities • Ensure compliance with GCP, SOPs, regulatory requirements, and sponsor expectations • Foster accountability across study teams while creating an environment of collaboration, transparency, and shared ownership • Contribute to process improvements and operational best practices that enhance study execution and team performance

• Function as a member of the study-specific project team including understanding the systems, providing support related training of the systems and is responsible for the completion of all support related project deliverables • Partner with functional area leads and senior peers to identify and evaluate fundamental issues on projects • Gather information regarding potential or actual risks/issues and provide detailed information to management to ensure risks/issues are surfaced and mitigated • Serve as the primary contact for sponsors and study team members during maintenance • For moderately complex systems, perform study specific informal testing, create and review study specific system support guidelines for accuracy and completeness • Prepare, coordinate and deliver meeting materials and communications per timeline milestones • Attend/facilitate meetings and communications with sponsors, vendors and cross-functional team members • Serve as a support escalation contact for study-specific questions/issues

Role Description CarePoint Response is seeking an experienced and compassionate Prescriber to provide psychiatric evaluation, medication management, and clinical consultation services within our behavioral health programs. - Conduct psychiatric evaluations and diagnostic assessments. - Provide medication management and ongoing psychiatric treatment services. - Support medication-assisted treatment (MAT) and recovery-oriented interventions. - Participate in overdose prevention and response initiatives, including targeted naloxone distribution. - Provide psychiatric consultation to nurses, clinicians, and allied healthcare professionals. - Collaborate with interdisciplinary treatment teams to ensure continuity of care. - Support coordinated treatment planning across behavioral health programs. - Maintain accurate, timely, and compliant clinical documentation. - Ensure services comply with SAMHSA guidance, federal and state regulations, and organizational policies. - Utilize precise, objective, and person-first clinical language in all documentation and communications. - Support quality improvement initiatives and regulatory compliance efforts. Qualifications - Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO). - Current unrestricted Maryland medical license. - Active DEA registration. - Active Maryland Controlled Dangerous Substances (CDS) registration. - Previous psychiatric practice experience required. - Leadership experience in evidence-based crisis intervention services preferred. - Strong psychiatric assessment and medication management skills. - Excellent clinical judgment and decision-making abilities. - Exceptional written and verbal communication skills. - Ability to prepare clear, objective, and regulatory-compliant clinical documentation. - Proficiency with electronic health records (EHR) and data-driven clinical practice. - Commitment to trauma-informed, recovery-oriented, and person-centered care. Benefits - Comprehensive Benefits Package: 100% employer-paid healthcare premiums for most available medical plans, including Dental, Vision, Life Insurance, Long-Term Disability (LTD). - 403(b) Retirement Plan. - Generous Paid Time Off. - Professional Development & Continuing Education Opportunities. - Collaborative Clinical Leadership Environment. - Mission-Driven Work That Changes Lives.

• Manage biomarker related operational work for clinical trials and programs. • Act as biomarker operation representative to lead/participate in cross-functional activities and initiatives. • Act as key vendor liaison to manage vendor relationship, resolve account level issues and improve processes. • Oversee and manage the performance of junior project managers. • Independently manage biomarker and bio-sample testing activities for clinical trials. • Oversee lab vendor performance and act as key vendor liaison to resolve account level issues and improve collaboration and processes. • Collaborate and communicate with internal functional stakeholders to drive the biomarker related works for clinical trials. • Build collaborative relationships with cross-functional teams as biomarker operation representative and lead/participate cross-functional activities and initiatives. • Collaborate with internal teams to review key study documents and provide training to investigator sites as needed for sample collection schedule, sample processing and shipment. • Participate in clinical study team meetings and program meetings, providing updates and insights related to biomarker activities and progress. • Have a good knowledge of CDx regulations and manage three-way communications with both device partners and lab vendors.