Role & responsibilities Provides entry level administrative support to assigned Project Manager(s), as well as site management for all assigned clinical trials. Administratively assists with all assigned project activities, ensures protocol adherence, and addresses non-compliance issues, as appropriate. Partners with clinical sites to coordinate and execute site activation procedures, personnel training, equipment credentialing, and query resolution. Looks for and identifies trends or issues with site activities and escalates appropriately. Ensures sites have adequate training and arranges ad hoc training(s) with the appropriate subject matter experts when necessary to ensure ongoing quality imaging and standardization. Responsible for updating CTMS with Site and Subject information accurately and in a timely manner. Pulls weekly reports and trackers from CTMS as requested. Responsible for maintaining Clinical Trial Records and performing scheduled assessments in a timely manner. Responsible for timely filing all project documentation and key correspondence for assigned trials. Responsible for study closeout record e-transfer transfer/shipments Assists PM with the coordination of internal, sponsor and other meetings, as needed and upon request. Creates study specific draft documentation, as well as weekly meeting agendas and minutes for PM. May provide administrative support during project-related audits. Assists with all other departmental requests as needed and upon request. Preferred candidate profile 2+ years administrative support experience, or similar, required. Clinical Trial experience or knowledge a plus Proficient in Microsoft Word, Excel, PowerPoint, and experience using database software Excellent organizational skills and attention to detail Strong written and verbal communication skills Proactive and ability to work independently. Flexible and able to manage multiple priorities and deadlines. Positive attitude, ability to work within a team environment. Perks and benefits Best in Industry

Role & responsibilities Capable of implementing applicable procedures and associated documents. Supports team members with the fulfillment of requests from Quality Assurance. Assists team with responding to and tracking the fulfillment of general requests to Read Services. Follows general Decision Tree guidelines when liaising externally. Under general supervision, uses software tools to facilitate document collaboration. Produces clean, final legal & regulatory documents from templates and enters data accurately into designated tracking systems while maintaining data type and formatting requirements. Assists with contract preparation, onboarding, and vetting of Readers/Consultants. Under general supervision, collects manual and electronic signatures in compliance with GCP. Tracks and updates time-sensitive documentation for active Readers/Consultants. Consistently follows mandatory naming conventions and file structure requirements. Manages database and department file store to ensure audit readiness. Maintains confidentiality of project, budget, and protected health information (PHI) in strict compliance with company procedures and policies and regulatory requirements. Participates in building Reader relationships through responsive interaction with institutions, Reader vendors, and individual physicians. Contributes to process improvement initiatives. Exhibits a team approach with a positive, flexible attitude toward work assignments and learning. Preferred candidate profile Degree or equivalent work experience is required. Experience in clinical research or imaging related field preferred. Excellent verbal and written communication skills in the English language. Proficiency with using MS Office software. Strong customer orientation. Ability to work independently, effectively organize and prioritize tasks, and meet deadlines in a dynamic environment. Good problem-solving skills. Accurate and detail-oriented.