Clinical Case Support Specialist

We are seeking an experienced Clinical Case Support Specialist to provide on-site and remote clinical trial support for our Investigational Device Exemption (IDE) studies involving a Sirolimus-Coated Balloon (DCB) in the cardiovascular domain (CAD and PAD). This role is pivotal in ensuring protocol adherence, clinical support and training during the cases, subject safety, and data integrity during case procedures while facilitating communication between investigational sites, sponsor teams, and CRO partners. Key Responsibilities Case Support & Site Engagement Provide on-site or on-line procedure support during investigational DCB angioplasty cases, ensuring adherence to study protocol, device handling SOPs, and ICH-GCP requirements. Act as the technical and clinical liaison between investigators, cath lab teams, and sponsor during case execution. Support subject eligibility verification, informed consent review, and device accountability in compliance with 21 CFR Part 812 and ISO 14155 standards. Document case-related observations, protocol deviations- if any, and procedural data in accordance with the monitoring plan. Clinical Operations & Documentation Assist in site initiation, training, and qualification activities related to IDE protocol. Maintain real-time records of procedural outcomes, adverse events, and device usage logs. Support CRA/monitoring teams with source data verification (SDV) and query resolution. Ensure compliance with regulatory, ethical, and sponsor-specific quality standards. Cross-functional Collaboration Work closely with R&D, Regulatory Affairs, and Clinical Project Management to provide field feedback and procedural insights. Participate in risk assessments, monitoring reviews, and data quality meetings. Provide training or refresher sessions to cath lab staff on investigational device handling, use of the Investigational device and Trial Protocol as needed. Qualifications & Experience Bachelor’s degree in Nursing, Biomedical Engineering, Life Sciences, or equivalent clinical field. Minimum 2-5 years of experience in clinical research, cath lab, or cardiovascular device and Clinical trials. Hands-on experience with angioplasty, stent, or drug-coated balloon interventions in CAD and PAD space. Familiarity with FDA IDE, ICH-GCP E6(R2), and EU MDR or other regional regulatory frameworks. Strong understanding of clinical trial documentation, source data verification, and informed consent processes. Preferred: Experience supporting interventional cardiology (CAD) and Peripheral artery disease (PAD) device studies or drug-device combination products. Prior role as clinical specialist, field clinical engineer, Cath lab nurse/technician, or clinical research associate in cardiovascular studies. Excellent communication and presentation skills with the ability to engage physicians and clinical teams. Strong situational awareness in cath lab environment. Attention to detail, documentation accuracy, and compliance mindset. Ability to travel to investigational sites across the US as required (up to 60%). Team-oriented, adaptable, and calm under procedural pressure. #J-18808-Ljbffr Concept Medical