Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Provides clinical training and support to customers, as a subject matter expert in dosimetry, on-site and/or remotely to ensure customer is prepared to operate their equipment according to a minimum of safe and effective use guidelines and to fully utilize the complex functionality of the technology to meet their business needs. Responsibilities: - Provides clinical applications training to customers both on site and remotely to ensure customer is well prepared to obtain training that will enable them to operate their Varian Medical System equipment according to a minimum of safe and effective use guidelines with the highest level of satisfaction. - Assist in managing the customer’s clinical expectations. - May coordinate or lead customer and/or employee training courses. - May conduct large group presentations at seminars, training programs, and trade shows. - Formulate complementary support training information in the form of quick tips, workbooks, video-media and implementation guides. - Work with cross-functional teams as necessary to support and enable best services and optimize customer relations. - Other duties as assigned by Training Operations and/or Applications Manager Minimum Required Skills and Knowledge: - Must be a Certified Dosimetrist. Additional RT License is preferred. - Travel required up to 75-100% and intermittent weekends. - Clinical understanding of the processes in a medical and/or radiation oncology department. - Successful applicant must also live in the Northeast region consisting of the following states. (Maine, New Hampshire, Massachusetts, Vermont, Rhode Island, Connecticut, New York, New Jersey, Pennsylvania, and Delaware). #LI-Remote Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. To find out more about Siemens Healthineers businesses, please visit our company page here. The base pay range for this position is: $99,930 - $137,401 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance. The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time. Position must have full access to Siemens Healthineers' client sites to perform the essential functions of this position. Many clients require Siemens Healthineers employees and representatives to meet certain Vendor Credentialing requirements before they will be allowed to have access to their sites. Unless prohibited by law, position must meet all Vendor Credentialing requirements necessary to have full client access and must continue to meet those requirements during the course of employment in this position. These requirements vary by client and may include, but are not limited to: Proof of valid identification (photo, driver's license, SSN) Criminal background checks Drug screens Immunizations (COVID-19, Hep B, MMR, Varicella, Influenza, Tetanus) Annual TB testing Healthcare training. Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law. EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, Click here. Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations. If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status. California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here. Export Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.” Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started. Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site. To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.

About the role The Associate Internal Clinical Research Associate (iCRA) is responsible for supporting and coordinating clinical study activities in accordance with applicable regulatory guidelines, sponsor requirements, and organizational standard operating procedures. The Associate iCRA plays a key supporting role to Clinical Study Managers (CSM) by assisting with overall study management and maintaining the study electronic Trial Master File (eTMF). The Associate iCRA plays a critical role in the project lifecycle of study start-up through close-out. The Associate iCRA ensures all activities are conducted in accordance with International Council for Harmonization Good Clinical Practice (ICH- GCP), and all other applicable regulatory requirements and guidelines. What you'll do - Assist with the management of study mailboxes, ensuring timely responses where needed and appropriate filing into the eTMF. - Support preparation of protocols, case report forms, IRB/EC submissions / documents. - Assist with site qualification and site initiation visits in collaboration with clinical operation teams. - Support study start-up activities including but not limited to collection, review and tracking of essential documents. - Work directly with sites to ensure all requirements are met prior to sites being activated. - Assist with maintenance and the development of study trackers (site contacts, FAQ log, training, payment reconciliation, etc.) - Assist with the preparation of project communications, such as newsletters and team presentations, to update stakeholders on study progress and operational status. - Maintain the eTMF for assigned studies and ensure that they are audit ready. - Assist with the study close-out process on a site level and study level. - Work closely with Clinical Study Manager, Monitors, study teams, clients, and sponsor representatives to ensure seamless study execution. - Assist with internal team meetings as required. - Participate in process improvement initiatives, SOP updates and functional working groups. - Participate in the development of tools and templates that benefit the broader iCRA team. - Assist with audits and inspections. - Perform other duties as assigned. Qualifications - Bachelor’s degree in life science, data science, or related field. However, a combination of experience and/or education will be taken into consideration. - Minimum of 2 years of experience in clinical research. - Understanding of GCP, FDA, ICH, and other regulatory requirements related to Clinical Research - Excellent attention to detail and problem-solving skills. - Good communication and interpersonal skills. - Healthy disdain for the status quo. - Proficiency in data monitoring software and other relevant tools such as EDC. LOCATION AND TRAVEL REQUIREMENTS: This is a fully remote position and may be performed anywhere within the United States of America. Occasional domestic travel may be required for company meetings, audits, etc. This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Labcorp is seeking a remote Clinical Trials Project Manager to join our team! Work Schedule Monday - Friday, Day Shift Job Responsibilities - Ensure successful delivery of assigned clinical trial projects by aligning study specifications and deliverables with client, protocol, and internal requirements. - Clearly document and manage project scope, timelines, and expectations. - Coordinate cross‑functional activities including logistics, specimen management, data management, and laboratory operations. - Direct timelines and resource needs with relevant internal departments. - Ensure all validation and quality control requirements are met and documented according to SOPs and obtain all necessary internal and client approvals. - Organize and lead client meetings and training sessions; maintain complete documentation of all training. - Provide day‑to‑day project management through internal and external coordination throughout the project lifecycle. - Troubleshoot issues related to specimens, result reporting, and site compliance; provide timely resolutions or escalation as needed. - Monitor project progress through regular team meetings and provide updates and metrics to management. - Proactively identify project risks and escalate issues following global escalation policies. - Maintain consistent, clear communication with clients and internal leadership on project status. - Manage manual invoicing processes to ensure accuracy and alignment. - Collaborate with Quality Assurance during audits, inspections, and other QA/QC activities; respond promptly to information requests. - Complete all tasks in compliance with SOPs and policies and maintain required training documentation. - Support process improvement initiatives, standardization efforts, and SOP development or review. - Perform additional duties as assigned by management. Minimum Qualifications - Bachelor’s Degree in science, laboratory, or health related disciplines - 2 years or more of clinical trials experience - 2 years or more working within Microsoft Office applications Preferred Qualifications - 5 years or more years’ experience in a clinical trials environment - 1 year or more years’ experience working in LCLS, Salesforce, Periscope and Link Additional Job Standards - This position requires excellent written and verbal communication skills, strong organization skills and mindfulness, time management and prioritization skills, negotiation skills, presentation skills, and the ability to work in a fast-paced team environment. About Labcorp At Labcorp, we are a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development laboratory capabilities, our nearly 70,000 employees combine cutting-edge innovation, science and technology to solve some of today’s biggest health challenges, accelerate life-changing healthcare breakthroughs and impact lives around the world. Here, you are empowered to own your career journey and create a personalized development plan with the support of your team. Application Window: March 10, 2026 - March 13, 2026 Pay Range: $65,000 - $85,000 All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.  Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

• Leading the design and execution of clinical studies, ensuring adherence to protocol and regulatory requirements. • Collaborating with cross-functional teams to develop study protocols, informed consent forms, and study reports. • Analyzing clinical data and interpreting results to support decision-making and regulatory submissions. • Providing scientific input and strategic guidance throughout the clinical development process. • Establishing partnerships with key stakeholders to ensure alignment on study objectives and outcomes.