The Research Coordinator in the Clinical Trials Unit assists and collaborates with the Principle Investigator (PI) and research collaborators to reach research goals. This position requires a degree of responsibility, flexibility, and independence to perform diverse duties including collecting, analyzing, and archiving data.

The Research Coordinator will provide support, under the direction of faculty, for funded research projects for neuroimaging

The Scheduling Coordinator I will be responsible for all Patient Services Specialists’ duties and scheduling patient appointments, collecting patient and treatment information, communicating cost estimates, which includes patient liability along with helping to establish and coordinate payment arrangements.

The Scheduling Coordinator I will collect patient and treatment information, estimate deposit requirements, provide cost estimates, determine patient liability, establish payment arrangements, and coordinate payment arrangement information for outpatient and day programs with non-par payer sources.  

The Scheduling Coordinator I will collect patient and treatment information, estimate deposit requirements, provide cost estimates, determine patient liability, establish payment arrangements, and coordinate payment arrangement information for outpatient and day programs with non-par payer sources.  

The SchedulingCoordinatorIIwill ensure timely, accurate, and complete scheduling services for patients. This position follows the established protocols considering availability, priority, and appropriateness when scheduling appointments for patients and providers.    This position is on-site at our Baltimore, MD campus.

The Scheduling Coordinator II will schedule new and follow-up patient appointments for the Center for Autism Services, Science, and Innovation (CASSI, formerly known as the Center for Autism and Related Disorders, or CARD). The incumbent will perform a wide variety of administrative and front end clinical operations activities which include, but are not limited to greeting and checking in/out patients and families; collecting patient and treatment information; estimating deposit requirements; providing cost estimates; determining patient liability; establishing payment arrangements; and will coordinate payment arrangement information for outpatient and day programs with non-par payer sources. This staff member will interact with patients, families, clinicians, and administrative staff in a courteous and professional manner.

The Scheduling Coordinator II (Achievements) will schedule new and follow-up screenings and patient appointments. The incumbent will perform a wide variety of administrative and front end clinical operations activities which include, but are not limited to greeting and checking in/out patients and families; collecting patient and treatment information; estimating deposit requirements; providing cost estimates; determining patient liability; establishing payment arrangements; and will coordinate payment arrangement information for outpatient and day programs with non-par payer sources. This staff member will interact with patients, families, clinicians, and administrative staff in a courteous and professional manner.   *This position is located in Odenton 

The Physical Therapist IV (Senior) will take on a multifaceted role that includes patient care, education, clinical research, and data quality improvement initiatives. The position demands a dynamic individual capable of developing and overseeing therapeutic programs, as well as guiding interdisciplinary teams and community partners towards achieving clinical excellence.

The Senior Research Coordinator in the Clinical Trials Unit will be primarily responsible for complex project management for multiple research studies related to psychiatric conditions in pediatric patients. Activities include but are not limited to project execution, implementation, daily administration and close out for multiple research studies.  The Senior Research Coordinator will ensure precise implementation of and adherence to study protocol, create all study documentation, oversee operating procedures, timelines, IRB applications, data preparation, and other research-related activities. In addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment.