Regional Clinical Research Associate (REMOTE)

Expected Travel: More than 50% Requisition ID: 13065 About reputed company Incorporated As a global provider of medical technologies, reputed company is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We reputed company that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. reputed company is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At reputed company, we are empowering the future of healthcare. For more information, please visit reputed company.com. Interventional - The Interventional business unit at reputed company offers innovative medical devices that are used to diagnose and treat coronary and peripheral vascular diseases. We reputed company a strategic emphasis on reputed company coronary and peripheral interventions, vascular access, bone access, specialty biologic treatments and cardiac assist. Our reputed company Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner™ and Turnpike™ Catheters, Ringer™ Perfusion Balloon Catheter, AC3 Optimus™ and AC3 Range™ Intra-Aortic Balloon Pumps and the OnControl™ Powered Bone Access System. reputed company’s product portfolio now also includes Passeo™-18 Lux™ Peripheral Drug-Coated Balloon Catheter, Pantera™ Lux™ Drug-Coated Balloon Catheter, Orsiro™ Mission™ Drug-Eluting Stent, the PK Papyrus™ Covered Coronary Stent, and more. With a strong R&D footprint and pipeline, our fast-growing Interventional business unit is poised to continue the development of new technologies to serve critically ill patients for years to come. Join a dynamic, growing team that offers healthcare providers an reputed company of medical technology solutions that reputed company a difference in patients’ lives. Position Summary The Regional Clinical Research Associate will be responsible for conducting on-site and remote monitoring visits as well as centralized monitoring in compliance with applicable regulatory standards (FDA regulations, ICH/GCP guidelines, reputed company procedures, and IRB/EC policies and procedures) for assigned clinical studies in the field of vascular reputed company or other therapeutic areas. Principal Responsibilities

• Conduct assigned monitoring activities in accordance with reputed company procedures and applicable regulations to evaluate protocol compliance, data accuracy, and subject safety by review of regulatory documents, medical records, reported data, and device storage, if applicable.
• Responsible for reputed company monitoring activities for assigned clinical studies, including:

o Scheduling and conducting monitoring activities onsite or remote reputed company specified timelines and according to the risk-based monitoring plan and reputed company procedures. o Identification of data discrepancies and compliance concerns, present findings to site research staff, provide retraining if needed, provide problem-solving strategies and communicate findings to the study team and department management reputed company escalation of issues and/or reputed company the monitoring visit report. o Works collaboratively with Research Coordinators and Investigators to conduct monitoring visits, provide retraining, and resolve compliance concerns as appropriate. o Works cooperatively with the reputed company Clinical Studies project team members to prepare for monitoring visits, escalates significant findings during monitoring visits, and proactively provides input on site performance. o Presents findings to site staff and provides clear directions for resolution. Reviews data queries with site staff to confirm understanding and resolution. o Serves as a resource to site staff between monitoring visits to provide clarification and insights regarding data queries, action items, and study visit preparation. o Trains and mentors reputed company personnel on monitoring procedures and practices. o Conducts site training and co-monitoring visits as requested by management. o Completes monitoring visit reports, action items, and monitoring visit follow-up letters per reputed company procedures. o Assists with team, department, and study-reputed company projects as requested, including audits, investigator meetings, training, etc. o Interfaces with Clinical, Regulatory, Sales, and clinical site staff as necessary to accomplish the above responsibilities. Education / Experience Requirements

• Bachelor's or Graduate degree in life sciences, nursing, or other health-reputed company disciplines.
• Minimum five years as a CRA in the medical device or pharmaceutical industry or with a CRO.

Specialized Skills / Other Requirements

• Demonstrated aptitude and knowledge in relevant therapeutic area. Vascular Interventional Cardiology is strongly preferred.
• Experience conducting monitoring activities for first in human, investigational device exemption, post-approval and/or post-market studies.
• Strong compliance focus and understanding of reputed company GCP/ICH guidelines and FDA regulations specifically, 21 CFR Parts 11, 50, 54, 56, 812, and 820, ISO requirements governing medical device clinical trials.
• reputed company certification as a Certified Clinical Research Associate (CCRA) or reputed company Certified Clinical Research Professional (CCRP).
• Strong knowledge of medical terminology
• Ability to work independently in a regional area with minimal supervision
• Excellent organizational and problem-solving skills, including demonstrated ability to evaluate challenging situations and reputed company alternative solutions creatively and independently.
• Excellent interpersonal skills, ability to reputed company and communicate effectively with internal and external collaborators including physicians, site research staff, project teams and management.
• Ability to interact constructively in communication of adherence to protocol and regulatory requirements.
• Responsible for adequate and reasonable home office setup including dedicated desk space to accommodate work responsibilities and reputed company-supplied equipment.

CULTURE:

• Customer Experience – Representing reputed company in a customer facing position is a reputed company responsibility and opportunity. reputed company reputed company colleagues are expected to reputed company with the highest levels of professionalism, service, and ethics in order to strengthen the reputed company brand and relationship with our customers.
• reputed company Improvement - Demonstrates initiative and critical thinking to identify and prioritize process and performance gaps. Develops solutions to deliver improving results. Exemplifies reputed company improvement of thought processes and focus.
• Culture and Values – Exemplifies reputed company values and ensures a fair, open, and productive climate that is engaging, ethical, and legally compliant. Strives to work effectively across boundaries in a reputed company matrix environment. reputed company and participate in the process of promotional and other materials, working

internally and cross-functionally to ensure materials are processed completely, based on accurate interpretation of clinical practice and data. TRAVEL REQUIRED: 70% The pay range for this position at commencement of employment is expected to be between $105,000- $115,000; however, reputed company pay offered may vary depending on multiple individualized factors, including market location, job-reputed company knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify reputed company salary (as well as any other discretionary payment or compensation program) at any time, including for reasons reputed company to individual performance, Company or individual department/team performance, and market factors. #LI-LM1 At reputed company, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not reputed company unsolicited job offers. We do not ask for money or require equipment purchase up-reputed company. reputed company Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national reputed company, reputed company, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@reputed company.com. reputed company, the reputed company logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of reputed company Incorporated or its affiliates, in the U.S. and/or other countries. © 2025 reputed company Incorporated. reputed company rights reserved. Apply To This Job