Title: FFL - Finance Analyst Location: Houston, TX, United States(Hybrid) Job Description: As a Finance Analyst here at Honeywell, you will play a vital role in analyzing financial data, supporting budgeting and forecasting processes, and providing insights to drive business decisions. You will collaborate with various teams to ensure accurate financial reporting and contribute to the financial health and growth of the company. You will work out of our Houston, TX location on a hybrid work schedule. In this role, you will impact the strategic financial planning and operational efficiency by delivering timely and accurate financial analysis that supports Honeywell's business objectives. KEY RESPONSIBILITIES - Analyze financial statements and data to identify trends, variances, and opportunities for improvement. - Support budgeting, forecasting, and financial planning activities across business units. - Prepare detailed financial reports and presentations for management review. - Collaborate with cross-functional teams to ensure alignment of financial goals and operational plans. - Assist in the development and implementation of financial controls and procedures. BENEFITS OF WORKING FOR HONEYWELL In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: click here however, this may be shortened or extended depending on business needs and the availability of qualified candidates. ABOUT HONEYWELL Honeywell International Inc. (Nasdaq: HON) invents and commercializes technologies that address some of the world's most critical challenges around energy, safety, security, air travel, productivity, and global urbanization. We are a leading software-industrial company committed to introducing state of the art technology solutions to improve efficiency, productivity, sustainability, and safety in high growth businesses in broad-based, attractive industrial end markets. Our products and solutions enable a safer, more comfortable, and more productive world, enhancing the quality of life of people around the globe. Learn more about Honeywell: click here THE BUSINESS UNIT Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status. Learn more about inclusion and diversity :click here YOU MUST HAVE - Experience in financial analysis, budgeting, and forecasting within a corporate environment. - Strong knowledge of financial reporting standards and accounting principles. - Proficiency in financial software and tools such as Excel, SAP, or Oracle for data analysis and reporting. - Ability to interpret complex financial data and provide actionable insights to support business decisions. - Experience with financial modeling and variance analysis to identify trends and risks. WE VALUE - Bachelor's degree in Finance, Accounting, Economics, or a related field. - Experience in the industrial or manufacturing sector is preferred. - Detail-oriented with strong analytical and problem-solving skills. - Ability to work collaboratively in a fast-paced, dynamic environment. - Familiarity with ERP systems and data visualization tools is a plus.

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients • Partners with study teams, AbbVie internal R&D stakeholders, investigators, and site staff for meaningful and effective engagements positioning AbbVie as the partner of choice in clinical trials • Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance to the protocol and monitoring plans • Gather local/site insights and utilize site engagement tools to report/track progress and measure impact of that strategy • Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance • Supports local onboarding of more junior CRAs • Responsible for activities as assigned by manager

• 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

• Oversee the operational aspects of clinical trial conduct at investigational sites to ensure data integrity, regulatory compliance, and adherence to Good Clinical Practice (GCP) guidelines. • Support multiple clinical trials across various therapeutic indications and monitor site performance, resolving issues, and facilitating communication between sponsor and site personnel. • Evaluate clinical trial resourcing requirements for qualification (SQVs), training (SIVs), monitoring (IMVs) and support of sites during the conduct of the trials. • Work with multiple trial sites and multiple studies of varying indications simultaneously. • Develop and maintain a monitoring plan for assigned clinical trial(s). • Liaise with external clinic and/or hospital investigators and associated staff conducting the trial as required. • Oversee the setup of the trial sites; ensuring each site has the appropriate trial materials to conduct the study. • Oversee site activation process for each study. • Periodically review data to identify potential issues or inconsistencies that could signal problems with data collection or monitoring. • Track patient enrollment and recommend solutions to trial site staff to increase appropriate enrollment of qualified subjects. • Provide support for the processing of data queries, deviations, adverse events, etc. • Write monitoring visit reports. • Develop and execute a plan to close trial sites on completion of the trial and perform associated close-out activities.