Clinical Trial Associate
The Clinical Trial Associate provides administrative support to the clinical research teams in the full spectrum of the research activities such as pre-clinical research, study start-up, study management and site closure.
Clinical research associates help to organize and monitor the different phases of clinical trials. Key responsibilities include:
Clinical Manager – Europe (Coronary & Peripheral Clinical Trials)
The Clinical Manager – Europe is responsible for planning, executing, and overseeing clinical trials for coronary and peripheral vascular medical devices across the European region. This role provides strategic and operational leadership to internal teams and external vendors (CROs, core laboratories, investigational sites, and distribution warehouses). The manager ensures that all clinical programs are conducted in compliance with ISO 14155, ICH-GCP, EU MDR, local country regulations, and internal company standards.
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.
Clinical Quality Specialist
We are seeking a skilled Clinical Quality Specialist with a focus on Quality Management Systems (QMS) to support IDE clinical trials. The ideal candidate will be responsible for establishing, managing, and maintaining QMS processes in compliance with clinical regulatory requirements. This role will ensure that all clinical trials and related activities meet high standards of quality, are GCP-compliant, and that internal and outsourced activities align with established QMS procedures.