Role Description This is a field-based position, supporting Abbott’s Vascular division. The Clinical Specialist will primarily be responsible for case planning, case support coverage, and product pull-through throughout the designated territory, and throughout the Region as needed. The Clinical Specialist will promote Vascular products through education, service, and training of customers in the hospital setting. The Clinical Specialist will provide clinical education and sales support in order to assist in achieving projected sales goals, increasing sales revenues within assigned product lines, and increasing market share. This position will have a heavy focus on Vessel Closure. What You’ll Work On - Serves as the technical procedure and product expert in support of case coverage in the hospital setting. - Meet with existing and potential customers (e.g., physicians, physician office groups at hospitals) to identify their clinical needs, goals, and constraints related to patient care and to discuss and demonstrate how Vascular products can help them to achieve their goals. - Develop relationships with hospital personnel; make new contacts in hospital departments; identify key decision makers. - Serve as primary resource for clinical support in case coverage, troubleshooting, and in-service education for company products. - Educate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using a wide variety of formats and platforms (e.g., slides, transparencies, manuals) to keep all customers abreast of the latest product, therapy, and technology developments and current items of interest in the industry. - Attend clinical procedures in the Cardiac Cath Lab, Interventional Radiology Lab, and Operating Room to ensure customer and patient success with Vascular products. - Respond to customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical research, marketing, product development) to develop optimal solutions. - Support the broader Region as needed with case support in addition to defined territory. Qualifications - Bachelor’s degree or equivalent combination of education and experience - 2-5+ years of related work experience - Ability to travel 50% within assigned region Requirements - Patient interaction experience within a lab/operating room environment - Relevant Technical Certification Benefits - Career development with an international company where you can grow the career you dream of. - An excellent retirement savings plan with high employer contribution. - Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. - A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. - A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

Role Description About Surgery: Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease, and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. We are searching for the best talent for Senior Specialist, Global Clinical Evaluation. The Senior Specialist, Global Clinical Evaluation will serve as an operational excellence subject matter expert across systematic literature reviews, clinical data appraisal and analytics, and medical/technical writing, supporting key deliverables including: - Clinical evaluation reports (CER) - Summaries of safety and clinical performance (SSCP) - Post-market surveillance reports (PMSR) - Periodic safety update reports (PSUR) - New product development (NPD) evidence generation strategies - Premarket approval (PMA) annual reports - Health Authority requests for all therapeutic areas / operating companies / platforms within the J&J MedTech Surgery business unit The Senior Specialist will translate strategy into execution by optimizing processes, standardizing tools/templates, and enabling scalable, efficient delivery models. You will be responsible for: - Driving continuous process improvement of Global Clinical Evaluation processes with a focus on improving, automating, and standardizing literature searching and reporting. - Creating and delivering training to Global Clinical Evaluation and other departments concerning the activities of Global Clinical Evaluation, results of activities, strategic/quality initiatives, etc. - Owning the end-to-end planning and execution of all assigned Global Clinical Evaluation deliverables (e.g., protocols, reports, regulatory responses). - Ensuring timely delivery of high-quality services and documentation as well as consistent deployment across MedTech Surgery. - Developing, implementing, and maintaining relevant procedures and templates, best practice and style standards, reference libraries, reviewer guidelines, and quality control tools/measures. - Managing the utilization and integration of platforms and software supporting systematic literature reviews including statistical analysis tools. - Identifying relevant stakeholders and implementing effective communication models. - Coordinating internal and external Medical Writing resources (writers, reviewers, project management, medical information specialists, librarians, vendors) to deliver against project goals. - Supporting the professional development of internal resources. - Actively partnering with Global Clinical Evaluation teams and cross-functional business partners such as Medical Directors, Medical Safety, Post Market Surveillance, Clinical Affairs, Design Quality Engineers, R&D, and Regulatory Affairs. - Providing technical review of data or reports to be incorporated into Global Clinical Evaluation deliverables and/or regulatory submissions to ensure scientific rigor, accuracy, and clarity of presentation. - Working with vendors/service providers to support the introduction of scalable tools, automation, and AI-driven solutions where appropriate. - Tracking key performance indicators, maintaining/monitoring metrics, and reporting issues or opportunities for improvement to leadership. - Ensuring the applicable writing processes are linked to appropriate Quality Systems and Regulatory Processes (e.g., Risk Management, PMS, etc.), supporting data/information accessibility. - Assisting in the management of the Global Clinical Evaluation budget including performing resourcing updates and approving invoices. Qualifications - BA/BS required; advanced degree preferred - 6+ years of experience in EUMDR, clinical evaluation reports, systematic literature reviews, or directly related regulatory/clinical field required - Demonstrated knowledge and experience in narrative or systematic literature reviews (e.g., PRISMA, Cochrane) with qualitative and quantitative synthesis in conjunction with scientific and medical writing required - Demonstrated knowledge and experience in clinical research methodologies with common biostatistical methods, systematic reviews and clinical data appraisal, and medical writing required - Experience with global medical device regulations and guidelines preferred - Change management expertise required - Knowledge of automation / artificial intelligence opportunities relative to medical/technical writing preferred - Regulatory/Notified Body front room audit experience preferred - Experience mentoring medical/technical writers, managing high-volume project work, and supervising internal and external writers/vendors preferred - Position can be performed remotely - 20% Domestic and International Travel required Benefits - Base pay range: $109,000.00 - $174,800.00 - Eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)) - Eligible to participate in the Company’s long-term incentive program - Vacation – 120 hours per calendar year - Sick time - 40 hours per calendar year; for employees who reside in Colorado – 48 hours; for employees who reside in Washington – 56 hours - Holiday pay, including Floating Holidays – 13 days per calendar year - Work, Personal and Family Time - up to 40 hours per calendar year - Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child - Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year - Caregiver Leave – 80 hours in a 52-week rolling period - Volunteer Leave – 32 hours per calendar year - Military Spouse Time-Off – 80 hours per calendar year

Role Description Working independently and following established policies, procedures, and study protocols, provides assistance on clinical research studies, including: - Collecting and organizing patient data - Maintaining and updating data generated by the study - Providing input into methodology design, statistical analyses, protocol design, and manuscript writing Essential Functions: - Participates in the design of research methodology - Plans, performs, and designs statistical analyses - Recommends protocol changes, writes protocols, and contributes to manuscripts - Independently performs specialized projects Qualifications - Bachelor's Degree Related Field of Study required or Graduate Diploma Related Field of Study preferred - Related post-bachelor's degree research experience 3-5 years required - Experience accepted in lieu of a degree - Ability to work more independently and as a team member - High degree of computer literacy and analytical skills - Ability to identify both technical and non-technical problems and develop solutions - Ability to interpret acceptability of data results - Highly proficient data management skills and working knowledge of data management systems - Able to display initiative to introduce innovations to research study - Excellent time management, organizational, interpersonal, written, and verbal communication skills Requirements - Remote Type: Remote - Work Location: 15 Parkman Street - Scheduled Weekly Hours: 20 - Employee Type: Regular - Work Shift: Day (United States of America) - Pay Range: $ - $82,014.40/Annual - Grade: 6 Benefits At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. In addition to competitive base pay, we offer: - Comprehensive benefits - Career advancement opportunities - Differentials, premiums, and bonuses as applicable - Recognition programs designed to celebrate your contributions and support your professional growth

• Responsible for the planning, execution, and reporting of data analysis for clinical and laboratory research • Partner with leadership and recommend solutions to improve department and team performance • Responsible for mentoring and training Statistician team/Medical Writing team • Generate statistical analysis plan (SAP) including sample size calculations and randomization schedules • Maintain the data management system for clinical studies and ensure compliance • Provide project oversight, training, and coaching