Clinical Research Operations Consulting
Build efficient operations.
Navigate compliance.
Scale with confidence.
LP Clinical Consulting partners with research organizations to optimize site operations, strengthen compliance, and build teams that deliver results — backed by 20+ years of hands-on clinical research leadership.
Lora Pea
I help clinical research organizations build efficient operations, navigate compliance, and scale with confidence.
With more than two decades in clinical research, my career has spanned the full continuum — from hands-on patient care as a Registered Nurse to executive leadership as Managing Partner at a multi-site research organization.
I've managed operations across 250+ clinical trials in CNS, dermatology, and metabolic therapeutic areas, covering Phase I through Phase IV studies. My work has included building teams from the ground up, negotiating complex Clinical Trial Agreements, and preparing sites for sponsor and regulatory audits — maintaining a track record of zero critical findings.
I bring a practical, operations-first perspective to every engagement. Whether you're launching your first site or optimizing an established portfolio, I focus on what actually works — proven frameworks, clear processes, and teams built to perform.
How I Work With You
Focused consulting engagements tailored to where you are and where you need to go.
Site Startup
Launch clinical research sites with operational frameworks refined across 250+ trials. From regulatory submissions to workflow design, I build the foundation for efficient, compliant operations from day one.
- Regulatory setup
- SOPs & workflows
- Staff onboarding
- Vendor coordination
CTA & Budget Negotiation
Strategic negotiation of Clinical Trial Agreements and study budgets. I protect your interests while maintaining productive sponsor relationships — ensuring fair terms and sustainable economics.
- Contract review
- Budget development
- Fair market value
- Amendment management
Pre-Audit Readiness
Comprehensive preparation for inspection-ready operations. I conduct gap analyses, remediate findings, and build quality systems that stand up to FDA, sponsor, and IRB scrutiny.
- Gap analysis
- Document remediation
- Mock audits
- Quality systems
Team Building
Recruit, train, and develop high-performing research teams. From defining roles to building training programs, I help you assemble the people and processes that drive results.
- Organizational design
- Recruitment strategy
- Training programs
- Performance frameworks
Career Background
A career built at the intersection of patient care, research operations, and executive leadership.
Managing Partner & Director of Clinical Operations
K2 Medical ResearchBuilt and led a multi-million dollar clinical research operation across multiple sites. Oversaw all aspects of clinical operations including team development, sponsor relationships, and business growth.
Senior Manager, Global Feasibility
ICON / AccellacareManaged global feasibility assessments across 112+ sites in 8 countries. Evaluated site capabilities, patient populations, and operational readiness for international clinical trials.
Director of Clinical Research
Olympian Clinical ResearchScaled the research team from 2 to 30+ staff members and managed 100+ clinical trials. Built operational infrastructure across CNS, dermatology, and metabolic therapeutic areas.
Academic Background
BS Psychology
University of Georgia · 2005
ASN Nursing
Hillsborough Community College · 2011
Professional Credentials
Registered Nurse (RN)
Florida Board of Nursing
Certified Clinical Research Coordinator (CCRC)
Association of Clinical Research Professionals (ACRP)
Let's talk about your
research operations.
Whether you're launching a new site, preparing for an audit, or scaling your team — I'd welcome the opportunity to discuss how I can help.