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Join Us in Shaping the Future of Clinical Research  Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change. At Adams Clinical, you’ll find: A culture of respect, transparency, and continuous improvement Opportunities for professional growth and learning A team dedicated to improving lives through innovation and integrity If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team. Job   Role   Adams Clinical is a rapidly growing research site network specializing in late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies.   The  Central Clinical Research Coordinator II  serves as a network-level operational lead  and  accountable owner for end-to-end study  success across   Adams Clinical's multi-site research network. This role  is responsible for  driving operational excellence from study activation through close-out by partnering closely with  site operations, central departments (e.g.,  Enrollment,  Quality, Regulatory), and sponsors  to ensure consistent study execution, enrollment success, data quality, and protocol compliance.   Reporting to the Senior Manager, Central Clinical Operations, the Central CRC II serves as the single point of operational accountability for study success across the research network. This role leads cross-functional collaboration to  monitor  study performance, standardize operational processes, proactively resolve operational challenges, and enable scalable, high-quality clinical research delivery.   Key Responsibilities:    Study Oversight & Execution   Hold end-to-end accountability for study success across the network, driving enrollment performance, data quality, site compliance, and  timely  milestone achievement from activation through close-out.  Continuously monitor  study health across assigned sites by reviewing enrollment performance, screening metrics, visit compliance, protocol deviations, query aging, data quality, and operational KPIs, proactively identifying and mitigating risks before they  impact  study outcomes.  Support database locks across sites, ensuring data queries, action items, and sponsor requests are addressed in a timely manner  to support successful database lock readiness.  Act as a network-level clinical operations consultant, traveling to sites (periodic travel)  to assess readiness f or  new stud ies , study expansions, increased enrollment, sponsor visits, and operational performance improvement initiatives.   Site Operations & Operational Excellence   Partner with Site Managers , site  study teams , and internal leadership  to develop and execute action plans that address operational risks, enrollment challenges, sponsor escalations  and  i dentify  operational gaps and implement corrective or preventative actions. Provides site-level oversight to ensure adherence to Adams Clinical procedures, study protocols, G CP , and sponsor expectations.  Lead operational readin