Role Description The Department of Medicine, Division of Hematology & Oncology has an outstanding opportunity for a Senior Clinical Trials Budget Specialist (Program Operations Specialist) to join their central administration finance team. Reporting to the Clinical Research Budget Manager and under the leadership of the Division Associate Administrator of Finance and Research, the Senior Clinical Trials Budget Specialist is responsible for implementing complex clinical research budgeting and revenue cycle strategy, development, and oversight across all Division Teams – including research faculty and staff – within the Division of Hematology and Oncology. This position oversees optimal revenue recovery and payment terms for investigator initiated and industry sponsored clinical trials, directing and training teams in revenue recovery, and ensuring regulatory compliance and fiscal accountability. Key Responsibilities: - Post Award Revenue Recovery - 80% - Perform comprehensive and independent review of patient activity, in comparison to the Clinical Trial Agreement, perform complex financial reconciliations to ensure full revenue recovery. - Using EMR EPIC, Clinical Trials Management Software (CTMS) OnCore, and financial system Workday, perform complex external sponsor invoicing, adhering to the terms of the Clinical Trial Agreement. - Manage and oversee the post award patient activity and billing review. - Interpret and analyze budgets both during active period and post closure, to provide feedback to budget building teams on areas of concern and strength. - Monitor and assess program compliance around clinical trial budget development. - Budget Development and Operations and Finance Management - 10% - Interpret, breakdown, and orient disease team staff to complex oncology clinical trial protocols. - Develop study-specific budgets that account for all procedural and labor costs. - Perform complex Medicare Coverage Analysis in accordance with Medicare Clinical Trial Policy. - Understand and interpret all institutional, state, and federal policies related to clinical research budgeting and billing. - Develop tools and metrics with the goal of increasing study budgeting process efficiencies. - Personnel Management - 10% - Direct the work of the Clinical Trial Post Award Specialists. - Support the Research Budget Manager with hiring, training and mentoring clinical trial post award specialists. - Train and mentor the clinical trial post award specialists. Qualifications - Bachelor's Degree in Business, Science, Health, or related field - Four years of experience with clinical research budget development, clinical research coordination, or related research or healthcare experience. Requirements - Experience with OnCore and EPIC - Demonstrated ability to work effectively and efficiently in a group environment. - Exceptional organizational and customer service skills. - Strong written and oral presentation skills. - Ability to communicate effectively with all levels of faculty, management and clinical research staff. - Demonstrated skill in using Microsoft Excel. Preferred Qualifications - Experience in an academic medical center, as a research study coordinator, and/or in oncology clinical research - Experience negotiating clinical trial budget and payment terms - Familiarity with interpreting regulatory and contractual documents. - Knowledge of the Medicare Clinical Trials Policy and other federal, state and institutional clinical research regulations - Experience with using ICD-9, CPT, and HCPCS billing codes in a clinical research environment - Strong working knowledge Microsoft Office Suite Working Conditions - Fast-paced office environment, with a high volume of often-complex projects. - The work is deadline driven and requires rapid and frequent communications. - This position is eligible to telework 100% remote. Compensation, Benefits and Position Details - Pay Range Minimum: $96,000.00 annual - Pay Range Maximum: $119,100.00 annual - Benefits: For information about benefits for this position, visit here . - Shift: First Shift (United States of America) - Temporary or Regular: This is a regular position - FTE (Full-Time Equivalent): 100.00% - Union/Bargaining Unit: Not Applicable

• Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval • Develops and implements regulatory strategies to obtain timely product approvals from worldwide regulatory bodies • Ensures regulatory submissions are accurately prepared and comply with regulatory approvals • Represents Medtronic from a clinical research perspective within the country / region and also collects feedback from local customers and authorities • Builds and maintains a strong network and close relationship with the various internal and external parties • Leads execution for both local and global studies, manages clinical research projects over all of the Medtronic therapies across multiple businesses

Role Description As a Sterilization Area Clinical Leader at Solventum, you will act as a strategic clinical advisor, partnering with internal teams and key customers to drive best practices and deliver advanced education. You will lead priority customer engagements, provide escalated clinical and technical consultation, and support economic value discussions with evidence-based data. You will make an impact by: - Acting as strategic advisor to internal Solventum teams on wound care clinical strategy and industry best practices - Collaborating with sales leadership to identify opportunities to educate and upskill teams and individuals on clinical or technical consultative practices - Presenting compelling data and clinical application during priority planned customer engagements - Building and maintaining relationships with key healthcare customers to ensure customer loyalty and satisfaction - Engaging alongside local teams to plan & lead comprehensive customer education events - Directly interacting with customers who require escalated consultation on clinical or technical on-label scenarios - Serving as a consultative partner to various internal business stakeholders on clinical and/or technical matters - Supporting economic objection handling with customers by articulating evidence-based clinical efficacy and the connection to economic value - Aiding in resource management for conversions/evaluations - Maintaining clinical/technical relevance through ongoing continuous learning and participation in professional associations - Understanding and translating current relevant industry standards (e.g., ERAS, AAMI) Qualifications - Bachelor’s Degree or higher AND 2 years of healthcare experience in a hospital, surgery center, or long-term care environment - OR High School Diploma/GED AND 4 years of healthcare experience in a hospital, surgery center, or long-term care environment - Experience with Microsoft Office applications (i.e. Excel, Power Point, Outlook) - Current, valid Driver’s License Requirements - Current certification(s): BSN, RN, CER, CRCST - Strong understanding of clinical value drivers across hospital care areas and alternative sites of care - Excellent organizational and time management skills - Understanding of the principles of adult learning - Demonstrated analytical, problem solving, project management, and implementation skills - Proven ability to cultivate strong internal and external collaborative relationships - Experience with public speaking and technical presentations Benefits - Competitive pay and benefits - Medical, Dental & Vision - Health Savings Accounts - Health Care & Dependent Care Flexible Spending Accounts - Disability Benefits - Life Insurance - Voluntary Benefits - Paid Absences - Retirement Benefits

Role Description As a Sr CRA in Oncology, you will be responsible for: - Performing site qualification, site initiation, interim monitoring, site management, and close-out visits (performed on-site or remotely). - Ensuring regulatory, ICH-GCP, and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. - Using judgment and experience to evaluate overall performance of site and site staff and providing recommendations regarding site-specific actions. - Maintaining a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. - Verifying the process of obtaining informed consent has been adequately performed and documented for each subject/patient. - Demonstrating diligence in protecting the confidentiality of each subject/patient. - Assessing factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site. - Conducting Source Document Review of appropriate site source documents and medical records. - Applying query resolution techniques remotely and on-site, providing guidance to site staff as necessary. - Utilizing available hardware and software to support the effective conduct of the clinical study data review and capture. - Performing investigational product (IP) inventory, reconciliation, and reviews storage and security. - Routinely reviewing the Investigator Site File (ISF) for accuracy, timeliness, and completeness. - Documenting activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents. - Supporting subject/patient recruitment, retention, and awareness strategies. - Understanding project scope, budgets, and timelines for own and others’ activities in the clinical team. - Acting as primary liaison with study site personnel, ensuring all assigned sites and project-specific site team members are trained and compliant. - Preparing for and attending Investigator Meetings and/or sponsor face-to-face meetings. - Providing guidance at the site and project level towards audit readiness standards. - May provide direct supervision, training, and/or mentorship to more junior level CRAs. - For Real World Late Phase (RWLP), supporting site throughout the study lifecycle from site identification through close-out. - Collaborating and building relationships with Sponsor and other affiliates, medical science liaisons, and local country staff. - Identifying operational efficiencies and process improvements. Qualifications - Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience. - Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. - Demonstrated good computer skills and ability to embrace new technologies. - Excellent communication, presentation, and interpersonal skills. - Moderate level of critical thinking skills expected. - Ability to manage required travel of up to 75% on a regular basis. Benefits - Career development and progression opportunities. - Supportive and engaged line management. - Technical and therapeutic area training. - Peer recognition and total rewards program. - Inclusive culture where you can authentically be yourself. Company Description Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change, and accelerate progress.