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As a Site Budget Specialist, you will play a critical role in the clinical trials budgeting process, driving the success of groundbreaking studies while ensuring compliance and efficiency.</p>\n<p>In this role, you will be part of the FSPx team and work directly with a renowned key sponsor to advance the development of innovative, life-changing medications.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Support Country Study site budget template, parameter, and payment term building to ensure timely setup of individual site budgets.</li>\n<li>Manage and execute assigned study site budget maintenance activities throughout the study lifecycle.</li>\n<li>Negotiate directly with globally assigned sites on master clinical trial agreements rate cards.</li>\n<li>Partner with the site payment department to ensure site budget and payment terms compatibility with payment systems and EDC requirements.</li>\n<li>Collaborate with internal Study Startup teams, Clinical Operations teams, and TAU partners to improve overall SB&amp;C metrics and implement processes.</li>\n<li>Ensure standards are applied to SB&amp;C processes across projects and portfolios, supporting continuous improvement activities while developing TA-aligned strategies.</li>\n<li>Leverage leading industry tools and data sources to provide budget and payment terms feedback aligned with parameters and fair market value guidance.</li>\n<li>Promptly recognise and improve potential delays, escalating non-performance.</li>\n</ul>\n<p><strong>Required Qualifications:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable (UK/EU).</li>\n<li>Equivalent relevant experience may be considered in lieu of educational requirements.</li>\n<li>2-4 years of experience in budget building, clinical research, or a related field.</li>\n<li>Strong understanding of ICH GCP guidelines and clinical research processes.</li>\n<li>Excellent negotiation, communication, and organisational skills.</li>\n<li>Ability to work independently and manage multiple priorities in a fast-paced environment.</li>\n<li>Proficiency in Microsoft Office and tracking systems.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Competitive salary and performance-based incentives.</li>\n<li>Flexible work arrangements (remote/hybrid options).</li>\n<li>Professional growth opportunities in a collaborative and innovative environment.</li>\n<li>The opportunity to work on cutting-edge clinical research projects.</li>\n</ul>","enriched_at":1793311569269},{"id":"job_d34ae5f1-159","title":"Senior Site Navigator","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Mexico-City/Senior-Site-Navigator_263260","location":"Mexico City","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>Senior Site Navigators play a critical role in coordinating site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.</p>\n<p>As a Senior Site Navigator, you will serve as the single point of contact for investigative sites, ensuring smooth progression from feasibility and initial outreach through to site activation, extending through the maintenance phase of the study as required.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Oversee site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs, and project requirements</li>\n<li>Identify potential research sites that align with the study&#39;s criteria and assess their capabilities and resources</li>\n<li>Conduct initial site outreach, collect Confidentiality Agreements, and feasibility surveys</li>\n<li>Support customization and translation of informed consent forms and patient-facing materials</li>\n<li>Collect, track, and perform quality reviews of essential documents required for effective and compliant study site activation</li>\n<li>Actively participate in study team meetings to support study progress and develop action plans for site level risks</li>\n<li>Support the CRA team in preparing for site initiation visits by coordinating with vendors, supplies teams, and study leads</li>\n<li>Perform initial contract and budget negotiations with sites</li>\n<li>Ensure high-quality documents are filed in applicable systems and the Trial Master File is updated and audit-ready</li>\n<li>Track the progress of the start-up process and ensure research sites meet all requirements and deadlines</li>\n<li>Serve as primary contact for investigative sites and ensure timely delivery in alignment with scope of work/study budget</li>\n<li>Perform Case Review Form (CRF) review and data validation against source documentation</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University/College degree (life science preferred), or certification in a related allied health profession, or 3-5 years&#39; work experience in clinical research</li>\n<li>Fluent in local official language and in English, both written and verbal</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Minimum of 3+ years of experience in clinical development or start-up/regulatory process</li>\n<li>Thorough knowledge of ICH/GCP, RA, IRB/IEC, and other applicable regulations/guidelines</li>\n<li>Demonstrated understanding of research protocol requirements and proven ability to communicate them</li>\n<li>Effective communication with various stakeholders, including site staff, CRO personnel, and regulatory authorities</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Remote-based work required with possible office presence depending on location</li>\n<li>Travel requirements: Limited for training only</li>\n</ul>","enriched_at":1793310521624},{"id":"job_eb32bd50-687","title":"Experienced CRAs","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Toronto/CRA-1-2---Sr-CRAs---Oncology---General-Medicine--French-Speaking-Desired--Canada_263916","location":"Toronto","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology experience is desired, and we are looking for candidates on the East and West Coast of Canada. French Speaking candidates are also desired. As a CRA, you will conduct 8-10 DOS per month, with potential travel across Canada.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Lead and support the Full Service Outsourcing team in monitoring clinical trials</li>\n<li>Conduct routine monitoring and close-out of clinical sites</li>\n<li>Maintain study files and ensure compliance with regulatory requirements</li>\n<li>Liaise with vendors and study site staff</li>\n<li>Ensure the protection of study patients and data integrity</li>\n<li>Perform CRF review, query generation, and resolution</li>\n<li>Assist with training of new employees and coordinate designated clinical projects</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession</li>\n<li>1-3+ years of Clinical Monitoring experience</li>\n<li>Oncology or ophthalmology experience is desired</li>\n<li>Open to various hub locations in Canada</li>\n<li>French Speaking preferred</li>\n</ul>\n<p><strong>Work Environment:</strong></p>\n<ul>\n<li>Fast-paced environment with changing priorities</li>\n<li>Teamwork and people skills are essential</li>\n<li>Technology-based with data collected directly into an electronic environment</li>\n</ul>\n<p><strong>Physical Requirements:</strong></p>\n<ul>\n<li>Ability to sit for extended periods and operate a vehicle safely</li>\n<li>Repetitive hand movement and ability to make fast, simple, repeated movements</li>\n<li>Occasional crouching, stooping, and lifting of 15-20 lbs</li>\n</ul>","enriched_at":1793309477776},{"id":"job_cfc6e3c3-137","title":"Executive Director, Quality Assurance and Regulatory Compliance","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Leeds/Executive-Director--Clinical-Pharmacology-Services-Quality-Assurance--United-States-or-United-Kingdom-_262686","location":"Leeds","job_type":"full-time","experience_level":"executive","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking an Executive Director, Quality Assurance and Regulatory Compliance to provide executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit.</p>\n<p>The successful candidate will ensure a robust, risk-based, and inspection-ready quality management system aligned with global regulatory expectations and Fortrea business strategy.</p>\n<p><strong>Core Accountabilities</strong></p>\n<ul>\n<li>Define and execute the QA strategy for the CPS business unit, aligned with enterprise quality objectives and business priorities.</li>\n<li>Establish and lead a risk-based quality management review process across CPS operations, including CPUs and supporting functions.</li>\n<li>Develop CPS-specific quality metrics, dashboards, and insights to drive proactive risk identification and continuous improvement.</li>\n<li>Ensure consistent interpretation and application of global regulations, including GCP and GMP requirements, within CPS.</li>\n<li>Provide executive QA oversight of Clinical Pharmacology Units (CPUs), ensuring inspection readiness and compliance with GCP, GMP, and applicable regulatory standards.</li>\n<li>Oversee QA frameworks governing GMP pharmacy operations within each CPU, including investigational product (IP) manufacturing, handling, labeling, storage, and accountability.</li>\n<li>Ensure robust controls across pharmacy processes, including chain of custody, temperature control, documentation, and reconciliation practices.</li>\n<li>Drive standardization and continuous improvement of CPU and GMP pharmacy quality systems, ensuring alignment across global sites.</li>\n<li>Support readiness for regulatory inspections and sponsor audits related to CPU and pharmacy operations.</li>\n<li>Establish and lead a risk-based quality oversight program for Phase IB/IIA trials conducted outside CPS clinics, including decentralized, hybrid, and site-based early-phase models.</li>\n<li>Develop fit-for-purpose QA frameworks addressing early-phase risks (FIH, dose escalation, adaptive designs).</li>\n<li>Implement proactive surveillance mechanisms (targeted audits, real-time quality signals, risk indicators).</li>\n<li>Standardize processes and oversight across non-clinic early-phase delivery models.</li>\n<li>Ensure alignment with Clinical Operations, Medical, and Safety.</li>\n<li>Embed quality-by-design principles into early-phase program design and execution.</li>\n<li>Provide executive oversight of compliance risks, escalation, and remediation strategies across CPS and early-phase programs.</li>\n<li>Ensure adherence to RC&amp;QA governance requirements and controlled documentation.</li>\n<li>Serve as delegate within the RC&amp;QA Leadership Team and contribute to enterprise governance forums.</li>\n<li>Partner with CPS and enterprise leadership to drive quality culture and execution.</li>\n<li>Influence strategic priorities and resource allocation aligned with CPS and early-phase delivery.</li>\n<li>Represent Fortrea externally as an SME in clinical pharmacology, GMP pharmacy oversight, and early-phase quality.</li>\n<li>Communicate quality strategy effectively to internal and external stakeholders.</li>\n<li>Lead QA teams supporting CPUs, GMP pharmacies, and early-phase programs.</li>\n<li>Develop workforce strategy including recruitment, capability development, and succession planning.</li>\n<li>Drive organizational change and continuous improvement aligned with evolving CPS delivery models.</li>\n<li>Provide strong performance management, coaching, and leadership development.</li>\n<li>Partner with stakeholders to manage QA budgets supporting CPS.</li>\n<li>Ensure efficient delivery of QA services aligned with quality, cost, and timeline expectations.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Extensive experience in a clinical trials regulated environment, including senior QA/Regulatory leadership roles.</li>\n<li>Strong expertise in GCP and GMP, particularly within clinical pharmacology and early-phase environments.</li>\n<li>Bachelor’s degree in Life Sciences (or equivalent experience); advanced degree preferred.</li>\n<li>Equivalent experience may be considered in lieu of formal education.</li>\n<li>Proven ability to define and execute QA strategies in clinical pharmacology, CPU operations, and GMP-controlled environments.</li>\n<li>Experience overseeing pharmacy operations supporting clinical trials (IP management under GMP).</li>\n<li>Demonstrated success leading global, matrixed teams.</li>\n<li>Strong executive presence with ability to influence internal and external stakeholders.</li>\n<li>Experience implementing risk-based quality oversight for early-phase trials.</li>\n<li>Strong track record in inspection readiness and regulatory engagement.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment</strong></p>\n<ul>\n<li>Ideally located at one of the Fortrea CPS units (Madison, WI - Dallas, TX - Daytona Beach, FL - Leeds, United Kingdom).</li>\n<li>Travel to CPUs, GMP pharmacies, and global sites as required.</li>\n<li>Flexibility for extended hours aligned with business and inspection needs.</li>\n</ul>","enriched_at":1793307716320},{"id":"job_4312cacd-cc9","title":"Site Navigators II","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/Site-Navigator-II_262438","location":"São Paulo","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.</p>\n<p>Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach through to site activation, extending through the maintenance phase of the study as required.</p>\n<p>A crucial component in meeting the requirements of the Site Navigator II role is ensuring regulatory compliance, robust site management, optimal site support and training, and effective collaboration between the sponsor, CRO, and clinical site staff.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Oversight of site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs and project requirements</li>\n<li>Identifying potential research sites that align with the study&#39;s criteria and assessing their capabilities and resources</li>\n<li>Conduct initial site outreach, i.e., site engagement, collection of Confidentiality Agreement, and feasibility survey</li>\n<li>Remote Pre-Study Visits and follow up documentation</li>\n<li>Support customization and translation of informed consent forms and patient-facing materials</li>\n<li>Collect, track and perform a quality review of all essential documents required for effective and compliant study site activation</li>\n<li>Actively participate in team meetings to facilitate study progress and implement action plans for site level risks</li>\n<li>Support the CRA team in preparing for site initiation visits (SIVs)</li>\n<li>Responsible for submissions to and liaise with applicable IRB/IEC, Third Bodies (if applicable), and Regulatory Authorities</li>\n<li>Perform initial contract and budget negotiations with the sites</li>\n<li>Ensure high quality documents are filed in applicable systems in accordance with SOPs and project requirements</li>\n<li>Track the progress of the start-up process and ensure that the research site meets all requirements and deadlines</li>\n<li>Ensure Fortrea is audit ready by completing accurate, timely, and consistent system compliance on an ongoing basis</li>\n<li>Serve as primary contact for investigative sites and ensure timely delivery in alignment with scope of work/study budget</li>\n<li>Perform Case Report Form (CRF) review and data validation against source documentation</li>\n<li>Perform country and site ICF review/customization, per local requirements</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution</li>\n<li>3+ years&#39; work experience in clinical research, including a strong working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations</li>\n<li>Fluent in local official language and in English, both written and verbal</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>A scientific degree and/ or clinical expertise is optimal for this role</li>\n<li>Minimum of 2 +year of experience in clinical development or start-up/ regulatory process</li>\n<li>Working knowledge of ICH/GCP, RA, IRB/IEC, and other applicable regulations/guidelines</li>\n<li>Demonstrated understanding of research protocol requirements and proven ability to communicate and educate others about them</li>\n<li>Effective communication with various stakeholders, including site staff, CRO personnel, and regulatory authorities</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Remote-based work required with possible office presence depending on location</li>\n<li>Travel requirements: Limited for training only</li>\n</ul>","enriched_at":1793307203904},{"id":"job_b7537332-700","title":"Senior CRA – UK national monitoring","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Senior-CRA_25113","location":"Maidenhead","job_type":null,"experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>As a Senior CRA at Fortrea, you will work across cutting-edge science in clinical research, contributing to a diverse and challenging portfolio that includes Oncology, Neuroscience, General Medicine, Cell &amp; Gene Therapy, and CAR-T Therapy Studies.</p>\n<p>Your role will involve leading and managing sites across varied and complex indications, building trusted relationships with investigators and study teams, ensuring patient safety and data integrity remain paramount, and actively contributing to innovative and first-in-class studies.</p>\n<p>Fortrea offers:</p>\n<ul>\n<li>Breadth of experience across multiple therapeutic areas</li>\n<li>Exposure to advanced therapies, including cell &amp; gene and CAR-T</li>\n<li>Supportive leadership and a culture of trust</li>\n<li>Career acceleration and skills development</li>\n</ul>\n<p>Requirements include:</p>\n<ul>\n<li>Monitoring experience in clinical trials</li>\n<li>Curiosity and comfort with complexity</li>\n<li>Strong communication and stakeholder skills</li>\n<li>A desire to grow your portfolio and career</li>\n</ul>","enriched_at":1793306887883},{"id":"job_89196aed-e05","title":"Site Navigator","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Taipei/Site-Navigator-I--SSU---IHCRA-_261006","location":"Taipei","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>Site Navigators play a critical role in coordinating site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities. As the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach through to site activation and maintenance phases of the study.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Oversee site-level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs, and project requirements.</li>\n<li>Identify potential research sites that align with the study&#39;s criteria and assess their capabilities and resources.</li>\n<li>Conduct initial site outreach, collect Confidentiality Agreements, and feasibility surveys.</li>\n<li>Apply independent judgment and discretion in managing site-level activities, resolving issues, and making decisions that support study timelines and compliance requirements.</li>\n<li>Perform remote pre-study visits and follow-up documentation.</li>\n<li>Support customization and translation of informed consent forms and patient-facing materials.</li>\n<li>Collect, track, and perform quality reviews of essential documents required for effective and compliant study site activation.</li>\n<li>Actively participate in study team meetings to support study progress and develop action plans for site-level risks.</li>\n<li>Support the CRA team in preparing for site initiation visits.</li>\n<li>Liaise with applicable IRB/IEC, Third Bodies, and Regulatory Authorities.</li>\n<li>Perform initial contract and budget negotiations with sites.</li>\n<li>Ensure high-quality documents are filed in applicable systems and the Trial Master File is updated and audit-ready.</li>\n<li>Track the progress of the start-up process and ensure that the research site meets all requirements and deadlines.</li>\n<li>Serve as the primary contact for investigative sites and ensure timely delivery in alignment with the scope of work/study budget.</li>\n<li>Perform Case Report Form (CRF) review and data validation against source documentation.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University/College degree (life science preferred), or certification in a related allied health profession, or 2-3 years&#39; work experience in clinical research.</li>\n<li>Fluent in local official language and in English, both written and verbal.</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>At least one year of experience in a related field (e.g., medical, clinical, pharmaceutical, laboratory research).</li>\n<li>Basic knowledge of ICH/GCP, RA, IRB/IEC, and other applicable regulations/guidelines.</li>\n<li>Demonstrated understanding of research protocol requirements and effective communication with various stakeholders.</li>\n<li>Ability to manage multiple tasks and deadlines simultaneously.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Remote-based work required with possible office presence depending on location.</li>\n<li>Travel requirements: Limited to training only.</li>\n</ul>","enriched_at":1793306307912},{"id":"job_b2eb9f43-95a","title":"Clinical Operations Lead","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Senior-Director--Clinical-Network_263685","location":"Tokyo","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Clinical Operations Lead to oversee clinical operational activities and performance across a group of countries or delivery team. You will lead a team and be accountable for quality oversight and management, resource management, and financial delivery. You will also maintain a network of country ambassadors to drive strategic country growth.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Provide leadership to a team of direct reports and indirect reports across multiple countries</li>\n<li>Partner with Clinical Delivery Center of Excellence (CoE) and Project Delivery (PD) to drive organisational goals</li>\n<li>Attract, select, onboard, develop, and retain high-performing talent</li>\n<li>Represent Fortrea Leadership to external parties and customers within the country(ies) of responsibility and region</li>\n<li>Lead country and regional initiatives and participate in global initiatives</li>\n<li>Manage country expertise network to provide clinical expertise and insight</li>\n<li>Define strategies to improve operational efficiency, quality, and productivity</li>\n<li>Develop and execute country quality plans aligned to identified quality risks</li>\n<li>Manage budget spend and delivery aligned to project scope and profitability goals</li>\n<li>Identify business opportunities within country through proactive networking with customer stakeholders</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>University/college degree in life sciences or certification in a related allied health profession</li>\n<li>Expert level of English and local language required</li>\n<li>Thorough knowledge of drug development process and relevant SOPs, ICH, and GCP guidelines</li>\n<li>Ability to manage a team to ICH GCP/FDA/ISO14155 standards</li>\n<li>Demonstrated ability to lead by example and encourage team members to be responsible and accountable</li>\n<li>Excellent planning and organisational skills</li>\n<li>Strong financial acumen</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>Minimum of 10 years supervisory experience, including 2 years of managing managers</li>\n<li>1 year leading a team or function with 4 years experience of effectively managing customer relationships in a healthcare or clinical research setting</li>\n</ul>","enriched_at":1793306044493},{"id":"job_7c4e7bf6-43d","title":"Clinical Research Associate","source_url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Chengdu/FSP-CRA-I-II-Hefei-_256018","location":"Chengdu","job_type":"full-time","experience_level":"mid","work_arrangement":"hybrid","category":"Healthcare","description":"<p>We are seeking a Clinical Research Associate to manage and monitor clinical studies at various sites.</p>\n<p>The successful candidate will be responsible for ensuring that studies are conducted in accordance with Company and Sponsor Standard Operating Procedures, as well as Regulatory Guidelines.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Conducting routine monitoring and closeout of clinical sites</li>\n<li>Maintaining study files and conducting pre-study and initiation visits</li>\n<li>Liaising with vendors and other stakeholders</li>\n<li>Ensuring that study staff have received proper materials and 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audit readiness at site level</li>\n<li>Acting as a Lead CRA as assigned</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A university or college degree, or certification in a related allied health profession</li>\n<li>Thorough understanding of ICH GCP Guidelines and local regulatory requirements</li>\n<li>Knowledge of monitoring procedures and the clinical trial process</li>\n<li>Fluent in local office language and English</li>\n<li>At least 2 years of Clinical Monitoring experience</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Thorough working knowledge of Fortrea SOPs for site monitoring</li>\n<li>Additional years of experience in a related field</li>\n<li>Phase I monitoring experience</li>\n<li>Life Science or Nursing qualification</li>\n</ul>\n<p>The role involves travel, including air travel, which is an essential function of the job. 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