Clinical Research Assistant

Clinical Research Assistant This is an in-person job in Davenport, Iowa. Position Summary The Clinical Research Assistant (CRA) provides operational and participant support for clinical research studies conducted at the site. This positionassistsClinical Research Coordinators (CRCs), investigators, and study teams with participant scheduling, specimen processing, investigational product accountability support, supply management, and study-related documentation. The Clinical Research Assistant plays a critical role in ensuring efficient study conduct while allowing coordinators to focus on protocol management, participant care, and study execution. Essential Responsibilities Participant Support and Scheduling Coordinate participant appointments and study visits. Contact participantsregardingupcoming visits and study requirements. Assistwith visit preparation and participant flow. Maintain study calendars and visit schedules. Support participant retention activities. Study Operations Maintain research supplies and study materials. Order study-related supplies and equipment as directed. Monitor inventory levels andmaintainadequate stock. Trackexpirationdates of study supplies and research materials. Ensure study materials are organized and readily available. Specimen Processing and Shipping Process biological specimens according to protocol requirements. Prepare and package specimens for shipment. Complete shipping documentation and laboratory requisitions. Maintain specimen shipment records. Coordinate with central laboratories and couriers. Study Documentation and Logs Maintain temperature logs and equipmentmonitoringrecords. Maintain medication accountability logs and inventory documentation. Assistwith essential study documentation. Ensure logs are completed,accurate, and up to date. Support filing and organization of study records. Regulatory and Administrative Support Assistwith document collection and filing. Route study documents for review and signature. Support maintenance of regulatory binders and electronic regulatory systems. Assistwith study start-up and close-out activities. Quality and Compliance Follow protocol requirements, GCP, sponsor requirements, and site SOPs. Escalate protocol deviations, equipment issues, or documentation concerns. Participate in training and quality improvement activities. Maintain confidentiality ofparticipantand study information. Qualifications Education High School Diplomarequired. Associate's or Bachelor'sdegree ina healthscience, biological science, or related field preferred. Experience Previoushealthcare, laboratory, administrative, or research experience preferred. Experience handling specimens or laboratory procedures preferred. Knowledge, Skills, and Abilities Strong organizational skills. Ability to manage multiple priorities. Attention to detail and accuracy. Strong communicationand customer service skills. Ability to work independently and within a team environment. Proficiencywith Microsoft Office applications. Ability to learn CTMS, EDC, and sponsor systems. Physical Requirements Ability to stand, walk, and move throughout clinical areas. Ability to lift and transport study supplies and specimen shipments up to 25 pounds. Ability to perform repetitive computer-based tasks. #J-18808-Ljbffr