Clinical Research Study Assistant Optima DermatologyClinical Research Study AssistantBoardman, OHDUTIES AND RESPONSIBILITIES: Medical Receptionist: Welcomes and receives patients/visitors to Optima Research by greeting them with a warm, pleasant affect Provides study candidates and participants with appropriate forms for their visit Gathers information from study candidates/participants upon arrival using the appropriate form for their visit Notifies clinical staff when study candidates/participants are ready to be seen for their appointment Pulls and prepares study participant binders for scheduled visits the day prior In collaboration with the Clinical Research Coordinators, schedules study participant appointments within the visit window as designated by the study protocol in CRIO Provides study participants with appropriate compensation at the conclusion of each study visit, obtaining participant signature for cash distribution and maintaining stipend cash log Answers phones using professional telephone etiquette Knowledgeable of phone system and routes calls appropriately or takes detailed messages if call recipient is unavailable, documents messages in CRIO Notifies subjects of upcoming visits the day before Responds to and sends faxes Distributes incoming faxes to the appropriate recipient Knowledgeable in using front office equipment, such as copier, computer, etc. Complies with HIPPA guidelines, protecting and respecting the privacy of all patient information and records Stores all files in a permanent, dry, and safe location Maintains a cooperative, helpful, and pleasant affect, creating and/or contributing to an atmosphere of collaboration and team cohesiveness Maintains neatness of the front office, patient reception area, and patient lounge Cleans surfaces and chairs of patient reception area, patient lounge, and patient treatment rooms at the end of each business day with germicidal wipes Assists clinical research coordinators and other staff as needed Assists in the day-to-day operations, as needed and as assigned Clinical Trial Process: Assists in facilitating the daily clinical trial activities Reviews and comprehends each protocol Thoroughly and accurately completes study participant logs, keeping them current Assists in screening, recruiting, enrolling, and maintaining research participants Ensures adherence to protocol requirements Knowledgeable of the storage/temperature requirements for all assigned study medications stored on site Ensures appropriate specimen collection, processing, and shipment per study protocol Communicates lab alerts to appropriate persons in a timely manner.
Ignite Scholar, Research Assistant Professor Northeast Ohio Medical UniversityIgnite Scholar, Research Assistant ProfessorOHThis innovative program offers two dynamic tracks-Research and Graduate Education in Biomedical Science & Innovation, each tailored to provide the mentorship, resources, and support you need to thrive as a future leader in biomedical research or education. Upon successfully completing this two-to-three-year program and meeting professional benchmarks, you will be automatically appointed to a tenure-track assistant professor position-a seamless transition from early career scholar to full-fledged academic leader.
Coord Research & Education Mercy HealthCoord Research & EducationYoungstown, OHThis requires scheduling of last visit within an allotted time, physician needs to be onsite, review and determine if all study drugs have been returned or are accounted for, work closer with monitors to stay in line with study deadline, all data entry and queries completed, frequent onsite monitor visits, notify IRB and then box up all records according to guidelines. Accountable for the research department in maintaining and coordinating current and new research trials from gathering information on different trials, analyzes and proposes changes to the contracts and budgets, maintaining workflows specific to each trial, enrolling patients, to the close of each research trial.