• Serve as the primary operational lead for assigned studies, with accountability for enrollment performance, study quality, and overall execution across multiple sites • Partner with sponsors and CROs as a key point of contact, ensuring clear communication, alignment on expectations, and proactive management of study needs and concerns • Work directly with site teams to monitor enrollment progress, identify barriers to recruitment, and implement targeted action plans to improve performance • Proactively identify operational risks, including enrollment challenges and protocol-related issues; develop and execute mitigation strategies to keep studies on track • Drive accountability across sites by tracking and managing key performance indications (KPIs), including enrollment, screen failure rates, data quality, and timelines • Lead and facilitate study-related meetings with internal teams, sites, and sponsors/CROs, including kick-off meetings, enrollment reviews, and ongoing operational calls • Ensure timely and effective communication across all stakeholders, providing clear updates on study status, risks, and performance • Support study start-up, amendments, and ongoing trial execution by coordinating across functional teams to ensure efficient and compliant processes • Maintain accurate and up-to-date tracking of study timelines, milestones, and performance metrics within internal and external systems • Collaborate with Clinical Operations leadership to identify process improvement opportunities and implement solutions to enhance efficiency, quality, and site performance • Provide hands-on support to sites as needed, including onsite engagement, to address operational challenges and improve execution • Support the rollout and adoption of new processes, tools, and technologies that enhance clinical trial delivery

• responsible for working with the Clinical Operations team to deliver high-quality, client-centered, and profitable approaches to clinical startup services • proactively drives projects during the startup phase and interacts with clients as a startup subject matter expert • build and maintain strong client relationships and mutually beneficial long-term partnerships • lead and oversee clinical study startup teams and project start up activities • partner with Clinical Operations Leads, Project Managers, sponsors, and cross-functional teams to develop and execute effective startup strategies • actively drive study startup performance across site identification, feasibility, site selection, ethics/regulatory submissions, site activation, contract and budget negotiations, and essential document collection • ensure quality and completeness of startup deliverables by performing reviews of regulatory submissions, essential documents, startup trackers, and study records • monitor project startup timelines, KPIs, cycle times, and quality metrics • provide leadership, mentoring, and line management for Clinical Trial Assistants and Site Contracts/Budgets teams • perform business analysis and benchmarking within startup services and identify opportunities for continuous improvement

Title: Global Clinical Operations Manager Location: Remote Evendale time type Full time job requisition id R5033669 Job Description Summary The Global Clinical Operations Manager provides international clinical leadership and operational oversight for occupational health services across multiple aerospace facilities. This role is accountable for clinical operations, regulatory and medical compliance, program implementation, and contract performance across all clinics and non-clinic (NOSM) sites in the region. The Global Clinical Operations Manager partners with the Medical Director, EHS, HR, and Site Leadership to execute the global strategic plan, standardize occupational health programs, and ensure high-quality, compliant services that optimize employee experience, health outcomes, and business performance. This position will require up to 50% travel (including global travel) the first 1 - 2 years. Job Description Roles and Responsibilities: Regional/International Clinical Leadership & Governance - Lead and oversee clinical operations and compliance of occupational health services for all sites (clinics and NOSM sites) - Implement and enforce global and regional medical compliance programs, aligning with GE Aerospace expectations, OSHA and other country-specific regulations, ADA, DOT, HazCom, local health departments, data privacy and other health guidelines - Interpret and apply government rules and regulations globally/regionally that affect employees and clinic operations - Support and help execute the Health Services Strategic Plan developed with department leadership focusing on employee experience, quality outcomes, and safe, efficient service delivery Multi-Site Program Implementation & Compliance - Implement and execute compliance programs at all sites (clinic and NOSM) in line with global standards and local regulations - Administer, implement, and review all medical surveillance (MSE) programs, AED programs, and corporate medical scorecard metrics across the region. - Standardize medical compliance, medical surveillance protocols, clinic processes, and standard metrics across all sites - Conduct clinic audits and NOSM compliance reviews to assess performance against program requirements and regulatory expectations EMR / Systems Leadership & Data Management - Act as Superuser for the Electronic Health Record and other health IT applications (e.g., AED tracker, training trackers, safety/health frameworks) - Provide training and support to EHS teams and clinicians on health IT tools and documentation standards - Analyze and trend contract metrics, surveillance data, and clinical indicators, and report outcomes to the Global Clinical Lead, Medical Director, and business leaders Stakeholder Partnership & Strategic Support - Partner with Corporate, EHS, HR, Quality, and Site Leadership to ensure business compliance and execution of health services strategies and initiatives - Serve as a clinical/medical liaison for sites, collaborating with the Global Clinical Lead and other value streams on policy, regulation, and compliance topics - Partner with Crisis Management teams, acting as a consultant for Health Services during emergencies and business continuity events. - Support acquisition/merger integration as a Health Services consultant, particularly regarding clinic operations, compliance, and employee health programs Contract, Budget & Vendor Oversight - Provide oversight for regional/international clinic service contracts and global health/wellness contracts as delegated (e.g., ISOS, AED program), ensuring service quality and alignment with strategy - Analyze contract performance metrics and drive corrective actions where needed - Support management of budgets and schedules for health services initiatives in accordance with organizational goals Regional/International Team Support & Capability Building - Support the Executive Global Health Services Lead in coordinating Regional/International Clinic Leads or site-level clinicians, ensuring consistent execution of global standards - Provide onboarding for clinic and No on Site Medical (NOSM) sites regarding medical compliance programs, health services processes, medical surveillance exams, EMR use, etc. - Manage and train cross-functional teams (EHS, HR, site leaders) on health services programs, regulatory compliance, and metrics Required Qualifications: - Bachelor’s Degree from an accredited college or university (at least a BSN Preferred; Registered Nurse with current, unrestricted licensure) - At least 5 years of managerial or team lead experience in occupational/industrial health or non-hospital health settings; experience in large, matrixed organizations and multi-site or international roles Desired Characteristics: - COHN strong preference; Master’s degree in Health Services, Public Health, or Health Administration desirable - Experience with TQM/Six Sigma/Lean strongly preferred - 8+ years of managerial or team lead experience in occupational/industrial health or non-hospital health settings; experience in large, matrixed organizations and multi-site or international roles - Technical: Experience with EMR/occupational health information systems, data tracking, analysis and trending, and reporting to program leads and operational staff. Skilled with Excel and PowerPoint - Regulatory: Training or experience in OSHA and other country-specific regulations, emergency medicine, ADA, DOT, HazCom, HSE or equivalent, data privacy, and disability management - Communication & Influence: Excellent oral and written communication; strong interpersonal and negotiation skills; able to communicate with medical professionals, health authorities, and internal stakeholders at all levels - Regulatory & Program Expertise: Expertise in regulatory compliance and implementation of large-scale programs; experience with program start-up, implementation, and execution in corporate environments - Leadership & Collaboration: Ability to prioritize and direct resources appropriately; manage and train cross-functional, multi-site teams; represent GE’s vision and customer focus with multiple internal customers - Analytical & Metric-Driven: Proactive, metric-driven, with strong data analysis capabilities; comfortable using metrics to drive decisions and report performance - Professionalism & Integrity: Focused on employee confidentiality and its application to regulatory compliance, disability, EHS, and HR; strong professional presence, goal-directed, and self-starting; highly adaptive to change and complexity - Humble: respectful, receptive, agile, eager to learn - Transparent: shares critical information, speaks with candor, contributes constructively - Focused: quick learner, strategically prioritizes work, committed - Leadership ability: strong communicator, decision-maker, collaborative - Problem solver: analytical-minded, challenges existing processes, critical thinker The base pay range for this position is $158,000.00 - 210,000.00. The specific pay offered may be influenced by a variety of factors, including the candidate’s experience, education, and skill set. This position is also eligible for an annual discretionary bonus based on a percentage of your base salary/ commission based on the plan. GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness. ​ GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a “Sponsor”). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor’s welfare benefit plan or program. This document does not create a contract of employment with any individual. This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3)). Additional Information GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: No #LI-Remote - This is a remote position

Title: Director, Clinical Research Operations Transformation Location: Orange, NJ Full Time Hybrid Job Description: ABOUT VITALIEF Vitalief is a trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients.​ POSITION OVERVIEW We are seeking a highly experienced, strategic yet hands-on Clinical Research Operations Leader to join our delivery team as a full-time, fully benefited employee. In this role, you will partner with a multi-location community hospital system to transform its research enterprise into a scalable, high-performing, world-class clinical research operation. As the primary subject matter expert (SME), this leader will collaborate closely with the Vitalief delivery team to design and implement enterprise-level operational initiatives, with a strong emphasis on Non-Oncology programs and enhancing cross-system communication and coordination. A central focus of the role will be leading the operational build-out and execution of a Cardiovascular clinical trials pilot, including infrastructure development, staffing strategy, workflow optimization, and technology deployment. WHY VITALIEF? - Professional Growth: Join a team of experienced practitioners who bring both business acumen and domain expertise. - Impactful Work: Contribute to scientific advancements that directly improve patient lives. - People-First Culture: Thrive in an environment that fosters growth, innovation, and collaboration. - Comprehensive Benefits: Enjoy 20 PTO days, 9 paid holidays, company-paid life insurance, short- and long-term disability, a 401(k) retirement plan, and robust healthcare options. - Flexible Work Location: Hybrid role with 2–3 days per week onsite in the Orange, NJ area. - Competitive Compensation: Base salary, performance bonus, and equity incentives. KEY RESPONSIBILITIES - What Success Looks Like: - Successful design, launch and operational stabilization of a scalable Cardiovascular research pilot across multiple hospital campuses and ambulatory sites. - Aligned research strategy with institutional priorities through close partnership with executive, clinical, and administrative leadership. - Established standardized workflows, SOPs and enterprise-wide performance metrics for research operations. - Strengthened investigator engagement and increased research participation across service lines. - Established scalable infrastructure and service line activation frameworks, in collaboration with investigators and sponsors, to reduce study activation timelines, enhance start-up predictability, and support sustainable research growth. - Successfully managed cross-functional initiatives within matrixed reporting environments and complex academic-clinical governance structures. - Transition from opportunistic research conduct to a deliberate, strategic, and scalable clinical research enterprise. QUALIFICATIONS - Bachelor’s degree required; Master’s degree in Clinical Research Administration, Public Health, Nursing, or related field strongly preferred. - Minimum of 7 to 10 years of progressive clinical research operations experience, including 3 to 5 years in leadership or management roles. - Experience building and launching a clinical research multi-location operation from scratch, enabling timely initiation of multiple studies across diverse therapeutic areas. - Demonstrated experience leading and supporting complex multi-site clinical research settings, including academic medical centers, affiliated and non-academic health systems, and disparate research locations. - Demonstrated experience managing complex drug, device, adaptive, or multi-arm trials. - Cardiovascular clinical research experience strongly preferred. - Expertise in study start-up optimization, IRB processes, and regulatory compliance. - Experience with CTMS platforms (e.g., OnCore) and Epic research integration. - Strong knowledge of research billing compliance and Medicare clinical trial requirements. - Proven ability to develop SOPs, quality systems, and performance dashboards. - Experience strong relationships with sponsors and CRO partners to enhance site reputation and repeat business opportunities. - Strong executive presence with the ability to influence across matrixed environments. - Demonstrated success leading operational transformation or research program development initiatives. PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.