Role Description The Manager Operations is responsible for overseeing the operational conduct of clinical trials at contracted medical institutions within a defined country or region in accordance with Milestone One contractual obligations. The Manager Operations provides leadership to Lead Site Coordinators and Site Coordinators, serving as a subject matter expert and escalation point for operational issues. This position plays a key role in staff development, process improvement, and continuous operational excellence. SCOPE OF RESPONSIBILITIES - Assesses feasibility of research protocols by reviewing clinical, operational, and resource requirements and recommending suitable trials for the medical institution. - Monitors the progress of budget negotiations and study activation timelines to support timely site readiness. - Manages the team of (Lead) Study Coordinators, oversees the quality and results of their work by monitoring and follow-up of study related reports, timesheets, site trackers and other operational tools to ensure satisfactory performance of the Milestone One team. - Drives process improvement and standardization of clinical trial operations in alignment with ICH GCP, regulatory requirements, MO1 Controlled Documents, by contributing to the development of operational guidelines, templates, and procedures. - Creates a work culture environment that promotes process transparency, accountability, and continuous learning. Qualifications - Associate degree in life sciences or similar. Business Management degree or certification is a plus. - Certifications ICH GCP Training - Minimum 5 years of clinical on the job experience, in a leadership position at a clinical research facility or Network experience is highly preferred. - Knowledgeable and direct experience in the full life cycle of clinical research activities from pre-award through close out. - Fluent use of English - Proficiency in MS Office - Valid category B driver’s license - Excellent communications skills - Excellent management skills, experience managing remote staff preferred. - Effective problem solving and result oriented - Accountable - Team leadership skills Benefits - Compensation: USD 115000 - USD 150000 yearly Company Description Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.

• 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.