Clinical Site Development Lead – Cardiac Trials

pulsebiosciences; United States; On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health insurance

401k retirement plan

Wellness program

Job summary

Pulse Biosciences in the United States is seeking a Sr. Manager, Clinical Site Development to lead identification, engagement, activation and performance support of clinical sites for IDE and post‑market programs.

You will work with investigators, clinicians and hospital staff to qualify sites, establish enrollment pathways, and address operational barriers, ensuring compliant, timely study execution. This field-based role requires experience in medical device trials and strong

Responsibilities

• Execute the clinical site development strategy across assigned sites and territories.
• 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.

Job description

Pulse Biosciences in the United States is seeking a Sr. Manager, Clinical Site Development to lead identification, engagement, activation and performance support of clinical sites for IDE and post‑market programs.

You will work with investigators, clinicians and hospital staff to qualify sites, establish enrollment pathways, and address operational barriers, ensuring compliant, timely study execution. This field-based role requires experience in medical device trials and strong