PSenior Clinical Specialist – Medical Device (Cardiovascular) /ppuTravel : /u 60–80% (domestic and international) /ppbLanguages : Fluent in English and local country language /b /ppOur client is a pioneering company in cardiovascular medical technology. They are seeking a Senior Clinical Specialist to support ongoing clinical studies and the broader implementation of their innovative therapeutic device. This role is ideal for candidates with a strong background in cardiac catheterization labs, clinical research, or medical device field support who are passionate about advancing healthcare and improving patient outcomes. /ppKey Responsibilities /ppbTraining Education /b /pulliCollaborate with site Principal Investigators to train staff on the safe and effective use of our client’s technology, ensuring sites become fully operational. /liliIdentify training gaps and provide remedial education to uphold safety and protocol compliance. /liliDeliver ongoing educational support tailored to each center, addressing staff turnover and new hires. /liliPresent updates on cardiovascular science, clinical trial progress, and related congress activities. /liliRepresent our client at relevant local and regional meetings. /liliOversee training and onboarding for new centres as part of future expansion and center-of-excellence development. /li /ulpbProctoring Clinical Case Support /b /pulliProvide on-site proctoring during initial clinical cases to ensure proper device usage in accordance with clinical investigational plans. /liliEvaluate when sites are ready for independent operation based on training completion. /liliMonitor procedural adherence and collect data on protocol deviations. /liliGuide clinical teams in setting up workflows that ensure consistent data and imaging quality, coordinating with CRAs and Core Labs as needed. /liliMaintain thorough proctoring documentation and provide continued clinical support where required. /li /ulpbRegulatory Compliance Support /b /pulliSupport internal and external audits and inspections at study sites. /liliEnsure complete and accurate record-keeping aligned with regulatory standards. /liliAdhere to local and international regulatory frameworks throughout clinical trial execution. /liliMaintain ongoing relationships with site PIs and clinical teams beyond procedural support. /liliIdentify and nurture key opinion leaders (KOLs), both within and outside current trial sites, in preparation for broader commercial adoption. /liliDevelop and expand a network of clinical advocates through education and strategic engagement. /liliLeverage cross-functional collaboration with internal teams including RD, leadership, and clinical operations. /liliIdentify high-potential centres for early technology adoption and future designation as centres of excellence. /liliEngage with national societies and KOLs to inform strategic market entry. /liliServe as the voice of the customer, ensuring patient and clinician needs remain central to internal decision-making. /li /ulpbProfessional Development /b /pulliCommit to continuous learning through scientific journals, congresses, and professional education. /liliStay informed on industry developments, including competitive technologies. /liliBuild a strong understanding of regional healthcare systems and market dynamics relevant to our client’s technology. /li /ulpbRequired Qualifications /b /pulliBachelor’s degree in Life Sciences, Nursing, or related healthcare field (Master’s preferred). /liliClinical experience in cardiac catheterization labs or as a Field Clinical Specialist in the medical device or pharmaceutical industry. /liliProven background in proctoring, training, and education. /liliExcellent organizational, interpersonal, and communication skills. /liliAbility to thrive in a fast-paced, independent, and collaborative environment. /liliWillingness to travel extensively (up to 80%) within the region and internationally. /li /ul #J-18808-Ljbffr