Role Description We are seeking motivated, detail-oriented individuals to join our team as WFH Travel Advisors. In this role, you will assist clients with planning vacations and coordinating travel arrangements including flights, hotels, resorts, cruises, and vacation packages — all from the comfort of your own home. No prior travel industry experience is required. Full training and ongoing support are provided to set you up for success from day one. This opportunity is ideal for individuals who enjoy helping others, staying organized, and playing a role in creating unforgettable travel experiences for their clients. Key Responsibilities - Assist clients with planning vacations and travel experiences - Research and book flights, hotels, cruises, and vacation packages - Coordinate travel arrangements based on client preferences and budgets - Provide destination information and travel recommendations - Communicate with clients regarding reservations and travel details - Issue travel confirmations, itineraries, and documentation - Work with travel suppliers and vendors to secure travel services - Respond to client questions and assist with travel-related concerns - Maintain accurate records of bookings and client information - Stay up to date on travel trends, supplier offerings, and destination updates Qualifications - Strong communication and customer service skills - Excellent organizational and time management abilities - Ability to manage multiple tasks while maintaining attention to detail - Comfortable using online systems and digital tools - Self-motivated and able to work independently in a remote environment - Interest in travel and helping others plan great experiences Requirements - Fully Remote (Work From Home) position - Flexible schedule - Full training and ongoing support provided

• Develop new features and functionality within the database design functional areas • Assist Clinical Data Management in planning, directing, and managing the clinical database design and maintenance process • Review the protocol and associated study reference materials • Maintain database design timelines • Follow up on regulatory requirements, industry trends, benchmarking, and best working practices • Design and review case report forms (CRFs/eCRFs) • Author and review the Data Validation Specifications • Develop and review User Acceptance Test (UAT) plans • Coordinate and oversee the UAT process • Design and review patient Case Report Forms and database schema • Test data capture/entry screens through UAT • Participate in EDC vendor’s technical learning and exchange meetings • Provide user training to CRAs on EDC systems • Contribute to the development and maintenance of the company’s database design procedural documents • Plan, manage, control and perform data processing activities for assigned projects • Review the Data Management Plan (DMP) • Review data, issue and resolve queries • Assist in resolving medical coding discrepancies • Cooperate with the Quality Assurance Department with quality control audits • Define and monitor clinical trial data flow and quality control processes • Accurately and efficiently validate electronically captured data • Write clear queries on missing data and data points failing pre-defined range checks • Develop and test SAS codes for clinical trial database logical checks and study specific monitoring reports.

• Design clinical database for new studies based on requirement specifications in various electronic data capture (EDC) systems • Perform post go-live changes (database modifications) based on updated requirement specifications in various electronic data capture (EDC) systems and provide impact assessment for modifications • Perform Unit Testing on database design, assist User Acceptance Test (UAT) activities, and address UAT findings • Set up and configure the development environment for new studies • Assist the creation of the Database Integration Specification (DIS) with other systems, provide Integration Technical Detail (ITD) as needed, program the integration, and assist the integration test • Support the Data Manager in investigating and addressing issues related to the database design • Review study design requirement specifications for assigned projects, ensuring the specifications adhere to EDC platform standards and Everest Standards • Maintain database design timelines and promote good project management practices • Follow up on regulatory requirements, industry trends, benchmarking, and best working practices in data management and database design by reading, participating in relevant training, and/or associated activities • Validate and disseminate real-time study monitoring reports to Sponsor and internal team members.

• Develop new features and functionality within the database design functional areas to increase the efficiency of database design at the study level, and to improve and enhance the company’s database design capabilities • Assist Clinical Data Management in planning, directing, and managing the clinical database design and maintenance process • Review the protocol and associated study reference materials to contribute to the development of the clinical database design project timeline • Maintain database design timelines and promote good project management practices • Follow up on regulatory requirements, industry trends, benchmarking, and best working practices in data management and database design by reading, participating in relevant training and/or relevant association activities • Design and review case report forms (CRFs/eCRFs) and setup electronic data capture (EDC) systems for clinical trials • Author and review the Data Validation Specifications for assigned projects • Develop and review User Acceptance Test (UAT) plans for clinical databases designed by other designers • Coordinate and oversee the UAT process for clinical databases • Design and review patient Case Report Forms and database schema • Test data capture/entry screens through UAT • Participate in EDC vendor’s technical learning and exchange meetings as well as other internal and external training meetings • Participate in trial Investigators Meetings and provide user training to CRAs on how to use EDC systems, and on Dataflow and Quality Control Processes • Contribute to the development and maintenance of the company’s database design procedural documents, work instructions, checklists and templates for all EDC systems • Provide input to all data management procedural documents • Plan, manage, control and perform data processing activities for assigned projects. These tasks are performed in a timely and accurate manner and in compliance with trial sponsors’ requirements • Review the Data Management Plan (DMP) for assigned projects • Review data, issue and resolve queries • Assist the Lead Data Manager, sponsor or Investigative Site with resolving queries • Assist in resolving medical coding discrepancies resulting from coding of medical history, adverse events, procedures and medicinal products • Cooperate with and assist the Quality Assurance Department with quality control audits on assigned databases • Validate and disseminate real-time study monitoring reports to sponsor and internal team members • Define and monitor clinical trial data flow and quality control processes in accordance to corporate SOPs, Good Working Practices, and unit guidelines • Accurately and efficiently validate electronically captured data • Write clear queries on missing data and data points failing pre-defined range checks and/or logical checks • Participate in and contributes to Clinical Data Management initiatives • Develop and test SAS codes for clinical trial database logical checks and study specific monitoring reports