• Develop clinical trial budgets, including review of protocols and relevant documents to ensure that appropriate costs and allocation of institutional resources are fully captured in the budget. • Work in collaboration with ancillary teams, departments, investigators, research staff, supporting administration, and sponsors/funding agencies to create complete, comprehensive, accurate and timely budgets. • Ensure appropriate research rates are applied to study budgets. • Independently develop, negotiate, and finalize budgets of moderate complexity with sponsors, academic sites, and other extramural funding sources to reach an agreement on budget and payment terms. • Submit and maintain the budget and other financial information into OnCore Clinical Trial Management System (CTMS) to maintain proper reimbursement and revenue integrity. • Perform pre-award quality assurance to verify completion of required elements prior to Medicare Coverage Analysis. • Communicate and meet with stakeholders to facilitate ongoing budget discussions and provide updates to relevant parties. • Use advancing knowledge to develop and disseminate clinical research education as needed in accordance with federal regulations, institutional policies, and specific protocol requirements. • Apply knowledge of clinical research to provide recommendations and direction to clinical research teams to ensure budgetary compliance throughout all phases of the Clinical Trial Financials Lifecycle. • Develop and support the formulation of program policies, procedures, and resources to establish and enhance clinical trial financials workflows. • Provide excellent customer service while maintaining accurate results in a fast-paced, deadline-driven team environment. • Engage in special projects and ad hoc duties as a member of the administrative team.

• Translates business requirements into business solutions; • Acts as liaison between departmental leaders, staff and information technology staff to design and configure business solutions to ensure business requirements have been met. • Works closely with stakeholders to define business requirements and with technical staff to develop solution alternatives and actively participates in defining objectives to support changing business needs and availability. • Coordinates IT troubleshooting and day to day activities within the department to ensure seamless and minimal downtime of hardware, software and reporting requirements. • May manage small to mid-sized projects/tasks and represent the department on larger enterprise-wide project teams. • Creates and maintains project schedules by developing project plans and specifications, estimating time requirements, establishing deadlines, monitoring milestone completion, tracking all phases of the project product/service lifecycle, providing timely reporting of issues that impact project progress, coordinating actions, and resolving conflicts. • Coordinates and conducts project team meetings regularly to review project deliverables and deadlines. • Has knowledge and experience in the various techniques to elicit, analyze and communicate requirements within assigned functional areas. • Establishes test plans, test cases and executes testing. • Assists with end user training. • Recommends information technology solutions to meet business needs and coordinates the planning, development, and implementation of these solutions.

Role Description As a Phone Research Specialist, you will contact businesses from a provided list to verify employee counts using a short, pre-approved script. Calls are brief—typically around 30 seconds—and are presented as independent market research. Your primary responsibility is to collect accurate information and document the results clearly. This role is ideal for someone who enjoys structured, repetitive work, communicates confidently over the phone, and maintains accuracy while handling a high volume of calls. This is a 3-month contract role with the opportunity for additional hours and a project extension. Duties and Responsibilities - Make outbound calls to businesses from a provided account list. - Follow a standardized call script to verify company employee counts. - Present each call as independent research in a professional and friendly manner. - Make up to five contact attempts per account before marking it complete. - Accurately record call outcomes, employee counts, and any relevant notes. - Maintain organized records to ensure results are easy to review and analyze. - Follow established workflows while meeting quality and productivity expectations. Project Scope - Approximately 2,000 accounts requiring employee count verification. - Initial quality assurance batch before expanding to larger volumes. - Three-month contract with work assigned in phases. - Opportunity for additional hours based on project needs and performance. Qualifications - Excellent verbal English communication skills. - Professional, friendly, and confident phone presence. - Comfortable making a high volume of short outbound calls. - Strong attention to detail when documenting call outcomes. - Able to work independently once trained on the workflow and script. - Organized and dependable with consistent follow-through. Preferred Qualifications - Previous experience in phone-based research, customer service, call center, or outbound calling. - Experience using spreadsheets or CRM systems to document interactions. - Familiarity with business research or data validation projects. - Experience working remotely in a structured, metrics-driven environment. Schedule - Part-time to start (20+ hours per week). - Opportunity for increased hours as the project scales. - Calls must be placed during U.S. Central Time business hours. Benefits - Permanent remote work flexibility. - Paid Time Off. - Health Maintenance Organization (HMO) coverage. - Annual performance bonuses. - Dedicated coaches offer an extra channel of support and skill-building. - Opportunities for professional growth.

Role Description As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: - Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. - Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. - Collaborating with investigators and site staff to facilitate smooth study conduct. - Performing data review and resolution of queries to maintain high-quality clinical data. - Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Qualifications - Bachelor's degree in a scientific or healthcare-related field. - Minimum of 2 years of experience as a Clinical Research Associate. - In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. - Strong organizational and communication skills, with attention to detail. - Ability to work independently and collaboratively in a fast-paced environment. - Willingness to travel as required (approximately 60%). Requirements - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: - Competitive base salary and performance related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. Benefits may vary depending on role and location. Company Description ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.