• Performs and manages investigator recruitment activities and assists with development of tools such as phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites in partnership with study team • May assist in identifying study sites by performing site feasibility and recruitment tasks, e.g., completing, disseminating, and reviewing responses to site recruitment questionnaires • Schedules internal and external meetings as required • Prepares Investigator Site Files including distribution to study sites (electronically or physically), coordination with shipping vendor, if required • Performs ongoing essential document collection and review, maintenance, and close-out activities, organizing and maintaining site level data in the trial master file (TMF) ensuring that sponsor and investigator obligations are being met and are compliant with ICH/GCP guidelines and applicable local regulations • Assist with sets up and maintains site-related data in applicable clinical systems according to procedures and guidelines. Utilizes the Clinical Trial Management System (CTMS) to ensure milestones and activities are accurately tracked • Acts as site contact/liaison for study and site management issues including addressing questions, assists with managing study supplies, and may support offsite central monitoring activities. Escalates issues and risks as needed • Ensures timely and complete data entry by site in EDC or any other system that requires data entry • Sends email blasts/newsletter, updates, and updated study core documents to study site personnel • Assists in providing logistics support in samples management and tracking, where applicable and in study supply management • Supports investigators and investigative staff in fulfilling obligations regarding local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements • Assists in data review inclusive of site level data review, resolutions provided by sites to queries, facilitates database closure and freezing procedures as per study plans • Assist with study tracking via the CTMS, Study specific trackers or Sponsor designated system to ensure that the study reporting is current, accurate and complete • Documents site and Sponsor contact and study interactions in a timely and professional manner • Assist in remote review of the electronical Investigator Site File, where applicable • Assists with, or if needed, conducts Investigational Product accountability, where applicable • Consults with project team members regarding study site issues • Provides quality review of the amended site level informed consent template • Follows up with sites for trial invoices and ensures the CTMS is accurately updated to allow the timely processing of Investigator Payments • May attend site visits as needed, supporting the CRA to ensure sponsor and investigator obligations related to the study documentation are being met and are compliant with applicable regulatory requirements and guidelines • May serve as an Independent Essential Document Reviewer post-SIV • Supports on-site visit activities if needed • Provides team leadership, training, and assessment/ coaching feedback to in-house CRA team members • Leads multiple in-house CRAs on a project, providing training and mentoring as required • Assists management with the development of training materials • Assists project team with the development of study specific documents and procedures • May support manager and interface with partner departments to support enhanced project delivery • Participates in the creation and maintenance of clinical project documents including, but not limited to Clinical Monitoring Plans, Monitoring Visit Letter templates and Site Start-up Plans consulting with the CTM/SUL • May act or directly assist functional team lead in supporting sponsors (may have direct client interaction) clinical budget management, vendor support/management and evaluation of metrics to identify process improvements • May create and execute risk management strategies for their aspect of project delivery with oversight from functional team leads/functional managers • Performs other duties as assigned by management • Performs all tasks in accordance with applicable guidelines, (e.g., ICH-GCP), company and sponsor SOPs, project plan, study-specific processes, local regulatory requirements

• Provides overall support to study sites and clinical project teams engaged in clinical research studies • Acts as a point of contact for study sites • Works independently in providing support to CRA and sites • Assists with investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for evaluating investigative sites • Schedules internal and external meetings as required • Prepares Investigator Site Files including distribution to study sites • Performs ongoing essential document collection and review, maintenance, and close-out activities • Acts as site contact/liaison for study and site management issues including addressing questions • Ensures timely and complete data entry by site in EDC or other systems • Sends email blasts/newsletter to study site personnel • Supports investigators in fulfilling obligations regarding local submissions • Assists in data review inclusive of site level data review • Documents site and Sponsor contact and study interactions in a timely and professional manner • Provides training and mentoring to less-experienced team members

• Deliver engaging, individualized virtual instruction tailored to each student's goals, accommodations, and learning profile • Create structured lesson plans that align with student goals, grade-level standards, and the specific accommodations or modifications each student requires • Adapt instruction in real time based on student questions, progress, and engagement • Track student progress and communicate effectively with families and, where applicable, school district partners

Role Description We are seeking a motivated and detail-oriented Online Cruise Travel Coordinator to join our team. In this role, you will assist clients with planning cruise vacations by researching cruise lines, itineraries, cabin options, and onboard experiences. You’ll prepare customized quotes, organize travel details, and help ensure a smooth and enjoyable booking process from start to finish. This position is ideal for someone who enjoys planning, customer service, and helping others create unforgettable cruise adventures—all from a remote, home-based workspace. Key Responsibilities: - Research and recommend cruise itineraries, ships, cabins, and destinations - Prepare quotes, proposals, and complete travel itineraries based on client needs - Communicate with clients to gather details, provide updates, and answer general questions - Coordinate with cruise line partners and suppliers to confirm bookings and special requests - Maintain accurate client records, confirmations, and booking information - Provide exceptional service to ensure client satisfaction and a seamless cruise experience Qualifications - Strong communication and interpersonal skills - Excellent organizational skills with strong attention to detail - Proficiency with basic computer skills (email, web browsing, Microsoft Office or Google Workspace) - Ability to work independently, multitask, and meet deadlines - Reliable internet connection and a distraction-free workspace - Customer service, hospitality, or administrative experience is a plus but not required Benefits - Flexible remote work schedule - Supportive and collaborative team environment - Opportunities for growth within the travel and hospitality industry - Access to exclusive travel discounts and perks after meeting eligibility requirements - A rewarding role helping clients plan memorable cruise vacations