Senior Clinical Trial Manager - Electrophysiology

bostonscientific • Johns Creek, GA

6d • $125,800 - $239,000 • Hybrid

About The Position

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About the role: Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. As a senior clinical trial manager within Boston Scientific’s Electrophysiology business, you will lead the execution of a diverse and fast-moving portfolio of global clinical studies spanning first-in-human, IDE and post-approval phases. This role is designed for an experienced clinical leader who thrives in dynamic environments, pivots quickly as program needs evolve and consistently aligns execution with shifting clinical and business priorities. Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

Requirements

• Bachelor’s degree in a scientific, health care or related discipline, or a minimum of 8 years’ relevant clinical research experience gained through progressive roles in clinical trial execution (typically equivalent to full-time experience replacing a bachelor’s degree).
• Minimum of 8 years’ experience managing clinical trials or clinical programs, including global and/or multi-site studies across different phases of development.
• Demonstrated experience executing clinical trials in compliance with ICH-GCP, FDA and global regulatory requirements, including first-in-human, IDE and post-approval environments.
• Ability to travel up to 25%, including domestic and international travel as required.

Nice To Haves

• Advanced degree such as MS, MPH or PhD.
• Medical device clinical trial experience, preferably within electrophysiology, cardiology or rhythm management.
• Hands-on experience supporting first-in-human, IDE and/or post-approval electrophysiology studies, including atrial fibrillation or flutter ablation therapies.
• Strong ability to generate new ideas and approaches by applying creative thinking to complex and ambiguous problems.
• Strong ability to align execution with strategic goals and independently drive action amid changing priorities and limited direction.
• Strong ability to collaborate and influence across global, cross-functional teams with differing objectives and timelines.
• Strong ability to adapt quickly and remain effective under shifting clinical, regulatory and portfolio conditions.

Responsibilities

• Provide end-to-end operational leadership for global electrophysiology clinical trials, with accountability for study planning, execution and delivery across first-in-human, IDE and post-approval phases.
• Develop and maintain integrated clinical trial plans, including protocols, study-specific plans, timelines and risk mitigation strategies, ensuring alignment with clinical and program-level objectives.
• Serve as the primary point of accountability for day-to-day study operations, coordinating cross-functional activities and external partners to ensure consistent, high-quality execution.
• Lead oversight of CROs and vendors, including scope definition, performance monitoring, issue escalation and resolution to maintain study timelines, quality and compliance.
• Ensure clinical trial conduct complies with applicable regulations, ICH-GCP and internal quality systems, maintaining a continuous state of inspection and audit readiness.
• Identify, assess and proactively manage operational, regulatory and portfolio-level risks, adjusting execution strategies as studies evolve or priorities shift.
• Drive preparation and delivery of clinical trial status updates, risk assessments and decision-support materials for clinical leadership and cross-functional stakeholders.
• Support transitions between study phases (e.g., first-in-human to IDE, IDE to post-approval) by adapting operational plans, documentation and execution approaches to meet changing evidence-generation needs.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level