Title: Clinical Specialist (RN - Vascular Access) - Atlanta Location: Franklin Lakes, NJ, Atlanta, GA, United States Job ID R-548752 Category Sales Location Atlanta, Georgia Job Description: We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Job Description About the role: As a Clinical Specialist, you will play a crucial role in providing flawless clinical support and education to our valued customers. Join us and be part of a proven organization that strives for excellence in everything we do. The Clinical Specialist is a resource for the execution of the Medication Delivery Solutions value-added clinical business strategy. The role implements clinical programs and initiatives that differentiate the MDS product portfolio based on improved clinical outcomes and process enhancements which may result in a lower cost-in-use. The expertise and credentials of the Clinical Specialist enhances the credibility of recommendations to customers and strengthens customer service and support. This support to customers is achieved through recommending best practice and facilitating education. The Clinical Specialist actively engages in conversion management, product implementation and training of Medication Delivery Solutions products. The Clinical Specialist reports directly to the Clinical Manager. Works primarily in a geographically defined territory; however, based on clinical needs, could assist outside of the region. Key Responsibilities: - Manage responsibilities within the allotted Travel & Expense budget. - Provide monthly updates to the Clinical Manager on regional training activities and support provided in the region. - Facilitate customer training classes to support conversion or retention opportunities for key customers. - Collaborate with the Regional Team to clinically support customer engagements from pre-sale through post-conversion. - Develop strong working relationships with end-users while providing product in-servicing and clinical education. - Provide routine follow-up support to customers at end-user locations as needed. - Conduct regional training for contractual nursing support as needed. - Collaborate with the Clinical Manager and Regional Business Manager to optimize scheduling and activities for maximum results. - Conduct Vascular Access Management assessments programs to support both Vascular Care and Vascular Access sales organizations. Education & Credentials: - Associate of Science degree in Nursing required; bachelor's degree in nursing or science-based field preferred. - Active Registered Nurse (RN) license in good standing - Advanced certification in vascular access and/or critical care nursing preferred (such as CRNI, VA-BC, CCRN, CEN, or equivalent) Experience: - Minimum 3 years of clinical experience specializing in ultrasound-guided procedures and vascular access devices preferred (including PICC lines, midlines, and related technologies). - Demonstrated proficiency in patient assessment, device selection, and insertion techniques. - Possesses a strong understanding and knowledge of infusion therapy, vascular access, and key disease states served by MDS products. Additional Skills: - Excellent communication and training abilities for clinical education and customer support. - Ability to work independently and collaboratively with multidisciplinary teams. - Competence in troubleshooting and providing clinical expertise for BD vascular access products. - Proven training skills to conduct educational courses. - Persuasive and credible; able to influence without authority. - Ability to travel up to 70% of the time. - Must possess and maintain a valid state-issued driver's license and meet BD's auto safety standards At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. At BD, we are committed to supporting our associates' well-being, development, and success through a performance-based culture. For this position, BD offers a competitive compensation package along with the following benefits specific to this role: - Annual Bonus - Potential Discretionary LTI Bonus - Potential reimbursement of vehicle use/mileage - Potential reimbursement of phone use Health and Well-being Benefits - Medical coverage - Health Savings Accounts - Flexible Spending Accounts - Dental coverage - Vision coverage - Hospital Care Insurance - Critical Illness Insurance - Accidental Injury Insurance - Life and AD&D insurance - Short-term disability coverage - Long-term disability insurance - Long-term care with life insurance Other Well-being Resources - Anxiety management program - Wellness incentives - Sleep improvement program - Diabetes management program - Virtual physical therapy - Emotional/mental health support programs - Weight management programs - Gastrointestinal health program - Substance use management program - Musculoskeletal surgery, cancer treatment, and bariatric surgery benefit Retirement and Financial Well-being - BD 401(k) Plan - BD Deferred Compensation and Restoration Plan - 529 College Savings Plan - Financial counseling - Baxter Credit Union (BCU) - Daily Pay - College financial aid and application guidance Life Balance Programs - Paid time off (PTO), including all required State leaves - Educational assistance/tuition reimbursement - MetLife Legal Plan - Group auto and home insurance - Pet insurance - Commuter benefits - Discounts on products and services - Academic Achievement Scholarship - Service Recognition Awards - Employer matching donation - Workplace accommodations Other Life Balance Programs - Adoption assistance - Backup day care and eldercare - Support for neurodivergent adults, children, and caregivers - Caregiving assistance for elderly and special needs individuals - Employee Assistance Program (EAP) - Paid Parental Leave - Support for fertility, birthing, postpartum, and age-related hormonal changes Leave Programs - Bereavement leaves - Military leave - Personal leave - Family and Medical Leave (FML) - Jury and Witness Duty Leave Salary ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary offered to a successful candidate is based on experience, education, skills, and actual work location. Salary ranges may vary for Field-based and Remote roles. $85,537 - $141,135 (Range includes Annual Base + Incentives) Why Join Us? To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. To learn more about BD visit https://bd.com/careers. Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics. Required Skills Optional Skills Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift NA (United States of America)

Title: FSP - Clinical Research Associate 2 Location: United States Job Description: Our FSP team is currently seeking Unblinded CRAs with 1-3 years of monitoring! Candidates must resided within the United States. 8-10 days on site per month being a mix of onsite and remote. Open to West coast, Central and East Coast major hub locations. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards. Responsibilities: - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned - - Responsible for all aspects of site management as prescribed in the project plans - General On-Site Monitoring - Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study - Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements - Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data - Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested - Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs - Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management - Assist with training of new employees, eg. co-monitoring - Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned - Perform other duties as assigned by management Requirements - University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) - 1+ years of Clinical Monitoring experience - 50-60% overnight travel The important thing for us is you are comfortable working in an environment that is: - Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue. - Changing priorities constantly asking you to prioritize and adapt on the spot. - Teamwork and people skills are essential for the study to run smoothly. - Technology based. We collect our data directly into an electronic environment. Work Environment: - Work is performed in an office environment with exposure to electrical office equipment. - Frequent travel to clients/ site locations with occasional travel both domestic and international. Physical Requirements: - Ability to sit for extended periods and operate a vehicle safely. - Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. - Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. - Ability to access and use a variety of computer software developed both in-house and off-the-shelf. - Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. - Regular and consistent attendance. - Varied hours may be required. - Target Pay Range: $100-115K based on job title #LI - Remote Applications will be accepted on an ongoing basis. Learn more about our EEO & Accommodations request here.

• Support study start-up activities (feasibility, site selection, regulatory submissions) • Assist in building and maintaining study timelines and plans • Coordinate investigator meetings and support site activation • Oversee day-to-day trial operations across sites/countries • Ensure compliance with ICH-GCP and regulatory requirements • Monitor study progress, enrollment, and data quality • Identify risks and escalate as needed • Ensure audit/inspection readiness and quality standards • Review clinical data and support reporting to sponsors • Contribute to study reports and documentation

Role Description Als Studienärztin / Studienarzt (m/w/d) unterstützt du die Durchführung klinischer Evaluationsstudien zur Validierung digitaler Gesundheitsanwendungen. Du arbeitest eng mit unserem interdisziplinären Sidekick-Team zusammen. Dein Fokus liegt insbesondere auf der medizinischen Vorprüfung, dem Screening und der Begleitung potenzieller Studienteilnehmer:innen. Du trägst damit entscheidend dazu bei, dass unsere Studien sorgfältig, patient:innenzentriert und in Übereinstimmung mit dem Studienprotokoll durchgeführt werden. - Vorprüfung der Vorauswahl und Screening potenzieller Studienteilnehmer:innen, um die Eignung gemäß Studienprotokoll sicherzustellen - Begleitung der Randomisierung, Planung elektronischer Fragebögen sowie Verwaltung studienbezogener administrativer Aufgaben - Enge Zusammenarbeit mit dem interdisziplinären Sidekick-Team, insbesondere mit Clinical, Research und Product - Regelmäßige Abstimmung mit dem leitenden Studienarzt / der leitenden Studienärztin bzw. Principal Investigator, um den Studienfortschritt in Übereinstimmung mit dem Studienprotokoll sicherzustellen - Sicherstellung hoher klinischer und wissenschaftlicher Standards während des gesamten Studienprozesses Qualifications - Abgeschlossenes Medizinstudium mit relevanter klinischer Erfahrung als Ärztin / Arzt - Erfahrung in der Durchführung klinischer Studien von Vorteil - Patientenzentrierte, empathische Kommunikation - Starke organisatorische Fähigkeiten und eine sehr sorgfältige Arbeitsweise - Hervorragende Kommunikationsfähigkeiten mit einer teamorientierten Einstellung - Leidenschaft für digitale Gesundheitslösungen - Hohes Engagement, ausgeprägte emotionale Intelligenz und Anpassungsfähigkeit an ein dynamisches Arbeitsumfeld Benefits - Eine sinnstiftende Tätigkeit an der Schnittstelle von Medizin, Forschung und digitaler Versorgung - Mitarbeit an Evaluationsstudien für digitale Gesundheitsanwendungen mit realem Versorgungskontext - Ein interdisziplinäres, engagiertes Team mit medizinischer, wissenschaftlicher und digitaler Expertise - Flexible Zusammenarbeit in Teilzeit - Remote-Arbeit innerhalb Deutschlands oder Zusammenarbeit am Standort Hamburg - Eine projektbefristete Tätigkeit für ca. 4–6 Monate - Die Möglichkeit, aktiv zur Weiterentwicklung evidenzbasierter digitaler Gesundheitsversorgung beizutragen Contact Information Frau Jeanine Metaschk