Sr. Manager, Clinical Site Development

At Pulse Biosciences, we are driven by purpose and innovation. • Our Mission: To build a viable Company that designs, produces, and commercializes nano-pulse technology to improve and extend the lives of patients. To solve the needs of patients, physicians, and healthcare providers with high quality and high reliability products and services, developed in accordance with rigorous scientific, engineering, and clinical standards. We exist to make a positive difference in the lives of patients, physicians, healthcare providers, shareholders and our Pulse Biosciences team members. • Our Culture: A community of creative, forward-thinking individuals tackling challenges with ingenuity and collaboration. • Our Commitment: Hiring the best and brightest minds to advance our world-class organization.

Pulse Biosciences (Nasdaq: PLSE): Join the Future of Bioelectric Medicine Pulse Biosciences is a novel bioelectric medicine company committed to health innovation that has the potential to improve the quality of life for patients. The Company’s proprietary CellFX® nsPFA™ (nanosecond Pulsed Field Ablation) technology delivers nanosecond pulses of electrical energy to non-thermally ablate cells while sparing adjacent noncellular tissue. The Company is actively pursuing the development of its CellFX nsPFA technology for use in the surgical treatment of atrial fibrillation and percutaneously in a select few other markets where it could have a profound positive impact on healthcare for both patients and providers. Visit pulsebiosciences.com to learn more. Why Join Us? At Pulse Biosciences, we are driven by purpose and innovation. • Our Mission: To build a viable Company that designs, produces, and commercializes nano-pulse technology to improve and extend the lives of patients. To solve the needs of patients, physicians, and healthcare providers with high quality and high reliability products and services, developed in accordance with rigorous scientific, engineering, and clinical standards. We exist to make a positive difference in the lives of patients, physicians, healthcare providers, shareholders and our Pulse Biosciences team members. • Our Culture: A community of creative, forward-thinking individuals tackling challenges with ingenuity and collaboration. • Our Commitment: Hiring the best and brightest minds to advance our world-class organization. What You Will Experience: • Culture and Purpose - Purposeful and rewarding work collaborating with bright and curious minds brings us together! • Innovative Environment - An environment that fosters innovation to take products from concept to human use quickly! • Growth Opportunities - Learning culture focusing on professional and personal growth and development that you can only get in a startup-like environment! • Comprehensive Benefits - A variety of health insurance plans and supplemental insurance options, and 401k retirement savings plan. • Ownership and Rewards - Stock options awards and Employee Stock Purchase Plan (ESPP) to share in our success. • Work-Life Balance - Enjoy paid time off, paid holidays, flexible work schedule and wellness program, including onsite gym and mindfulness classes. • Diversity & Inclusion - A commitment to providing a respectful work environment to our diverse workforce. About the Role The Sr. Manager, Clinical Site Development leads the identification, development, engagement, activation, and performance support of clinical sites for the Company’s IDE and post-market clinical programs. This field-based role works closely with investigators, research coordinators, physicians, nurses, hospital administrators, Field Clinical Engineers, and the In-House Clinical team to establish strong site relationships and support successful clinical study execution. The Sr. Manager, Clinical Site Development executes site development and enrollment-support activities within an assigned territory or group of clinical sites. The position evaluates potential clinical sites, develops investigator and referral relationships, supports site qualification and activation, establishes enrollment pathways, and addresses operational barriers that may affect study performance. The successful candidate will have experience in medical device clinical trials, clinical research, clinical site management, patient recruitment, cardiac surgery, electrophysiology, interventional cardiology, or a related healthcare environment. To Make an Impact, You Will: Clinical Site Development Execute the clinical site development strategy across assigned sites and territories, identifying, assessing, and prioritizing sites based on investigator experience, patient population, procedural volume, staffing, facilities, research infrastructure, and ability to meet study requirements. • Lead or support site feasibility assessments, qualification activities, and the collection and analysis of information needed for site selection. • Develop and maintain relationships with potential and active investigators, research coordinators, physicians, nurses, hospital administrators, and other clinical stakeholders. • Identify appropriate investigators, referral networks, and institutional partners for the Company’s clinical programs. • Develop site-specific engagement, activation, and enrollment-support plans. • Evaluate operational, staffing, referral, scheduling, and patient access barriers that may affect site activation, enrollment, or ongoing performance. • Recommend and implement practical, compliant solutions to address site development and enrollment challenges, with appropriate approval and oversight. • Maintain regular communication with prospective and active clinical sites and provide timely updates to senior management as directed. Site Activation and Enrollment Support • Lead or support site initiation, activation, and readiness activities in collaboration with the In-House Clinical team, Clinical Research Associates, Clinical Project Managers, CRO personnel, and site staff. • Establish and strengthen appropriate referral pathways among electrophysiology laboratories, cardiology practices, cardiac surgery programs, and other relevant clinical departments. • Support site teams in identifying potential trial candidates in accordance with the approved protocol and applicable regulatory requirements. • Coordinate patient identification, screening, and enrollment-support activities within the scope of approved training, delegated responsibilities, and Company procedures. • Attend high-priority site activities and clinical cases, as appropriate, to support coordination among the site, clinical team, and Company personnel. • Lead or support site education, investigator meetings, grand rounds, peer-to-peer programs, and other appr