Senior Manager, Clinical Reporting

Job Description

Senior Manager, Clinical Reporting | Boston Scientific

The Tone:
This is a hybrid role at Boston Scientific, requiring employees to work from our Marlborough, Massachusetts; Maple Grove, Minnesota; or Arden Hills, Minnesota office at least three days per week. Boston Scientific is a global medical technology leader dedicated to improving patient health by advancing science for life through innovative medical technologies. This role is crucial for developing and evolving clinical reporting capabilities, enabling informed decision-making across Clinical Operations, Medical Affairs, Regulatory Affairs, and executive leadership. It directly contributes to operational excellence, inspection readiness, and future advanced analytics initiatives.

The TL;DR
• Role: Full Time
• Type: Hybrid
• Location: Hybrid, Marlborough, MA; Maple Grove, MN; Arden Hills, MN
• Pay: $125800–$239000 yearly
• Team: Leads a team of Clinical Reporting professionals
• Mission: Owns the strategy, execution, and continuous evolution of clinical reporting capabilities to drive data-driven decision-making and operational excellence throughout the clinical trial lifecycle.
• Tech Stack: Microsoft Power BI, Tableau, Spotfire, SQL, Snowflake, CTMS, EDC, eTMF

What You’ll Actually Do
• Strategic Leadership: Develop and execute the Clinical Reporting strategy, ensuring alignment with Clinical Operations priorities and enterprise objectives.
• Reporting Modernization: Identify opportunities to modernize reporting through automation, self-service analytics, data visualization tools, and emerging technologies.
• Portfolio Oversight: Own the portfolio of operational and executive clinical reports, ensuring solutions meet business requirements while maintaining accuracy, consistency, and regulatory compliance.
• Team Management: Lead, mentor, and develop a high-performing Clinical Reporting team focused on operational excellence, customer service, and continuous improvement.
• Cross-functional Partnership: Build trusted partnerships across Clinical Operations, Clinical Data Management, Biostatistics, Medical Writing, Regulatory Affairs, and Information Technology.

The Must-Haves
• Background: Bachelor’s degree in Life Sciences, Computer Science, Information Systems, Business Analytics, Statistics or a related discipline. Strong understanding of clinical trial processes, GCP principles, and clinical quality requirements.
• Experience: Minimum of 8 years’ experience in Clinical Operations, Clinical Data Management, Clinical Reporting, Clinical Analytics or related functions within the medical device, pharmaceutical, biotechnology or health care industry. Minimum of 3 years’ experience leading high-performing technical or analytical teams. Experience working with clinical systems, including CTMS, EDC, eTMF and clinical reporting platforms.
• Skills: Demonstrated ability to lead cross-functional initiatives and influence stakeholders across business and technology organizations. Excellent communication, collaboration, and organizational leadership skills.
• Bonus: Master’s degree or equivalent experience. Experience developing executive dashboards using Microsoft Power BI, Tableau, Spotfire or similar data visualization platforms. Working knowledge of SQL, Snowflake, data warehousing concepts and modern analytics platforms. Experience implementing reporting governance, KPI frameworks and reporting automation initiatives. Agile, Project Management Professional (PMP) or other continuous improvement or project management certification. Experience supporting reporting transformation initiatives within a global, regulated medical device or life sciences organization.