Vice President of Clinical Research Development

Mangrove Management Partners

$140K — $200K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 10+ years of business leadership experience, particularly in clinical research operations.
  • 5+ years in leadership roles within a CRO, SMO, or sponsor-side research.
  • Strong background in device trial operations, preferably in vascular or related fields.
  • Experience with clinical partnerships across outpatient centers and hospitals.
  • Comprehensive knowledge of FDA and GCP requirements for device trials.
  • Entrepreneurial mindset suited for growth-stage environments.
  • Excellent communication and operational strategy abilities.

Responsibilities

  • Design and implement a strategy to evolve the OBL-based research program into a full-scale SMO/CRO.
  • Establish processes and governance for scalable multi-site operations.
  • Forge partnerships with hospitals, physician groups, and device manufacturers to enhance trial diversity.
  • Oversee site activation, compliance, and strategic planning across various clinical sites.
  • Enhance the operational infrastructure for clinical data management and oversight.
  • Identify and integrate new research sites and investigators beyond current operations.
  • Develop relationships with sponsors and CROs to attract high-quality device trial opportunities.

Benefits

  • Opportunity to lead the transition of a clinical research arm into a national SMO.
  • Leverage existing OBL research sites and reputable vascular device programs.
  • Collaborate with leading vascular specialists and a proactive management team.
  • Potential for performance incentives and shaping a new business unit from inception.
Full Job Description
About the Opportunity

Vascular Breakthroughs is seeking a dynamic and entrepreneurial executive to build and scale our existing clinical trials business.
Our current clinical research operations are embedded within eight Office-Based Laboratories (OBLs) and focus exclusively on vascular device trials. This role represents a unique opportunity to expand that platform-both geographically and across 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 Operations and Executive Chairman.

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
  • 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.
  • 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.

#Mangrove

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