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Shockwave Medical - Palo Alto, CA, United States - Hybrid

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Salary: USD 79,000 - 126,500 / annual

Johnson & Johnson is hiring a Field Clinical Specialist for Shockwave Medical Inc., a company pioneering Intravascular Lithotripsy (IVL) technology to treat complex calcified cardiovascular disease. This is a field-based role providing case support to physicians in peripheral and coronary interventional procedures, supporting both pre-market and post-market phases of product development. Key responsibilities include: - Provide physician and hospital staff training on safe and effective use of Shockwave Medical's IVL devices - Deliver procedural case coverage during interventional procedures - Present clinical study training materials based on investigational plans, including study protocols, instructions for use, and case report forms - Manage relationships with key study investigators and clinical leaders - Partner with clinical research colleagues on site re-training, data collection, and issue resolution - Handle administrative activities including training documentation, territory travel management, and budget oversight - Support clinical studies with device training and timely data collection - Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines The role requires significant travel (>50% of time) and field-based work across assigned territories, with flexibility to support other territories as needed. You'll work in a fast-paced environment managing multiple priorities while demonstrating strong organizational and critical thinking skills. Qualifications: - Minimum Bachelor's Degree in business, science, nursing, or related field (or equivalent experience) - Minimum 2 years' direct experience supporting interventional or surgical procedures in a hospital setting, OR 1 year of industry/hospital-based life sciences sales support experience - Working knowledge of clinical research, Good Clinical Practice (GCP), and regulatory compliance guidelines for clinical trials - History of effective collaboration with regulatory agencies through clinical studies and market releases - Product knowledge including product vigilance and medical device reporting - High attention to detail and accuracy - Proficiency with MS Office products (word processing, spreadsheets) - Finance and budgeting knowledge - Strong prioritization and organizational skills - Excellent critical thinking, influencing, and negotiation skills - Effective written, verbal, and presentation skills - Ability to work independently and on cross-functional teams - Demonstrated willingness to accept feedback and continuous improvement - Ability to manage multiple priorities in a fast-paced environment - Cardiovascular industry experience preferred but not required

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