Exp Sci Clin Dev NonMD

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Clinical Development & Research – Non-MD Job Category: Scientific/Technology All Job Posting Locations: Danvers, Massachusetts, United States of America Job Description: We are searching for the best talent for  Exp Sci Clin Dev NonMD. Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech #LI-Hybrid  This is a hybrid role available in Danvers Massachusetts within The United States. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. An pre-identified candidate for consideration has been identified. However, all applications will be considered.

Support protocol development and implementation by preparing supporting generation of study documents (consent templates, CRFs, visit guides) and tracking approvals and presentations under senior oversight. Act as day‑to‑day contact for study sites for routine queries; escalate scientific or regulatory questions to senior staff. Validate study data in EDC; perform routine data quality checks and flag discrepancies for follow‑up. Help prepare annual study reports, meeting materials, and investigator correspondence; take meeting minutes and manage action item follow‑up. Assist with site start‑up activities, regulatory binder maintenance, and documentation needed for audits. Support literature searches and preparation of background summaries to inform study materials and regulatory submissions. Contribute to drafting slides, abstracts, and sections of manuscripts under guidance from scientific leads. Collaborate with clinical operations, data management, biostatistics, and regulatory teams to ensure smooth study conduct.

Master’s degree in engineering, life science, or related field. Equivalent clinical experience may be considered. 0–2 years clinical research or healthcare experience; internship or academic clinical project experience is acceptable. Demonstrates a solid understanding of cardiology and cardiovascular space, including familiarity with medical devices. Familiarity with clinical research processes, basic regulatory concepts (informed consent, IRB), and EDC system. Proficient in biostatistics; familiarity with statistical software such as R, MATLAB or SAS. Strong written and verbal communication skills and attention to detail. Strong work ethic, self-motivated, team player with strong