• Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. • In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document management, monitoring project site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best practices. • In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and tools. • Represents the corporation by maintaining collaborative relationships with stakeholders.

Role Description We are seeking a detail-oriented and analytical Research Analyst to support business research, content management, data analysis, and project coordination activities. The ideal candidate will have experience working with large datasets, managing research-related initiatives, and delivering accurate, actionable insights to stakeholders. This role requires strong organizational skills, the ability to manage multiple priorities, and proficiency in Microsoft Office applications, particularly Excel and PowerPoint. - Conduct research and analysis to support business initiatives and strategic projects - Gather, organize, validate, and maintain large datasets to ensure data accuracy and integrity - Develop reports, presentations, dashboards, and research summaries for stakeholders - Support content management activities, including data tracking, documentation, and information organization - Coordinate and manage assigned projects, ensuring timelines and deliverables are met - Analyze trends, identify insights, and provide recommendations based on research findings - Collaborate with cross-functional teams to address business questions and research requirements - Maintain process documentation and support continuous improvement initiatives - Present findings and key observations in a clear and concise manner to business partners - Ensure compliance with established quality standards and operational procedures - Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives. Qualifications - 5+ years of relevant experience in research, project management, business analysis, clinical research, or related fields - Experience managing projects and working with large volumes of data - Advanced proficiency in Microsoft Office applications, particularly: - Microsoft Excel - Microsoft PowerPoint - Microsoft Word - Proven solid analytical and problem-solving abilities - Proven solid content management and organizational skills - Proven excellent written and verbal communication skills - Proven ability to work independently and manage multiple priorities in a fast-paced environment Preferred Qualifications - Bachelor's degree in any discipline - Experience in healthcare, clinical research, business research, or analytics environments - Experience creating reports and performing data analysis - Knowledge of SQL and/or Oracle databases - Demonstrated ability to learn new tools, systems, and business processes quickly - Demonstrated solid teamwork and stakeholder management skills Competencies - Analytical Thinking - Attention to Detail - Project Coordination - Data Management - Research Methodologies - Communication Skills - Collaboration and Teamwork - Time Management - Adaptability and Continuous Learning Work Schedule - Night shift alignment supporting U.S. business hours - Work-from-home arrangement, subject to business and location requirements

• Build proactive talent pipelines across Product, Engineering, Corporate, Merchandising, Marketing, Creative, and other business functions • Conduct market mapping to identify target companies, talent pools, and competitive landscapes • Research talent markets, competitor companies and talent pools • Build market intelligence to enable recruiters and hiring leaders to find exceptional, high-performing talent; Surface market insights, competitive intelligence, and hiring trends to recruiting partners • Leverage data and market intel to develop strong opinions on top feeder companies, schools and candidate backgrounds • Support high-priority executive and hard-to-fill searches with deep research and talent intelligence

• Considered as the primary point of contact for the investigative site • High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning • Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership • Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects • Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study (ies) • Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy • Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities • Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey • Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance • Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development • May participate in global/local task forces and initiatives • Responsible for activities as assigned by manager • Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues • Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution • Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach • Identifies, evaluates and recommends new/potential investigators/sites on an on going basis • Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel • Ensures audit and regulatory inspection readiness at assigned clinical site at all times • Manages investigator payments as per executed contract obligations, as applicable