Vice President of Clinical Research Development

 new clinical areas—by establishing a broader infrastructure and network capable of managing device-based trials in partnership with hospitals, health systems, and external investigators. The role will work closely with executive leadership, physician leadership, and current clinical trials leadership, including the Vice President of Clinical Research and Chief of Clinical Operations and Research.

Key Responsibilities

Strategic Development & Leadership
• Design and execute a comprehensive strategy to evolve the current OBL-based research program into a full-scale SMO/CRO.
• Define organizational structure, processes, and governance to support scalable, compliant, and efficient multi-site operations.
• Build partnerships with hospital systems, physician groups, device manufacturers, and early-stage device companies to broaden the trial portfolio.

Operational Expansion
• Oversee site activation, contracting, budgeting, and compliance functions.
• Lead site identification, activation, contracting, budgeting, and strategic planning across hospital systems, outpatient centers, and external investigator sites.
• Mature the existing functional architecture (clinical operations, regulatory, data, monitoring, site management, quality assurance, vendor management, etc.).
• Advance centralized operations for data management, monitoring, and regulatory oversight.
• Identify and onboard additional research sites and investigators beyond Vascular Breakthroughs' current footprint.

Business Development
• Develop relationships with sponsors and CROs seeking high‑quality, device-focused research sites.
• Build the commercial model, pricing structure, and growth strategy for the new SMO/CRO business unit.
• Represent Vascular Breakthroughs' research capabilities at conferences, advisory boards, and industry partnership forums.

Cross-Specialty & Device Trial Expansion
• Lead efforts to diversify research beyond vascular interventions into adjacent procedural or surgical device categories.
• Maintain focus on device trials while leveraging existing operational efficiency and physician expertise in outpatient procedural care.

Leadership & Culture
• Recruit, mentor, and develop clinical research and operations teams.
• Foster a culture of scientific integrity, regulatory compliance, and operational excellence.

Qualifications
• 10+ years of experience in business leadership, including at least 5 years (preferred) in leadership roles within a CRO, SMO, or sponsor-side research operations.
• Deep understanding of device trial operations, ideally with experience in vascular, endovascular, interventional radiology, or related device areas.
• Experience managing clinical partnerships across outpatient centers, hospitals, and integrated health systems.
• Strong knowledge of FDA and GCP requirements for device trials.
• Entrepreneurial mindset and ability to thrive in a growth‑stage organization.
• Exceptional relationship management, communication, and operational strategy skills.

Why Join Us
• Lead the transformation of an established clinical research arm into a national‑level SMO.
• Build on a strong foundation of eight OBL-based research sites and a proven vascular device research program with established scientists and investigators.
• Collaborate with top-tier vascular specialists and a data-driven management team focused on innovation and patient outcomes.
• Competitive compensation, performance incentives, and the opportunity to shape a new business line from the ground up.
• Please note that this role is expected to commute to the Burlington, MA office at least once a week*

Compensation

$140,000 - $200,000 per year. Negotiable based on skills and experience.

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About the Company:
Mangrove Management Partners