Starting at the site level gives me a perspective that supports the site, the study, and the study team as a whole. That blended experience shapes a more thoughtful, collaborative approach to monitoring and study oversight.
Value Rooted in Experience
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I’m not here to sell you extra services or push a full-service package you don’t need. As an independent CRA and clinical operations professional, my only job is to support your study, your sites, and your goals. You get honest guidance, transparent work, and monitoring that prioritizes data quality over billable hours.
Independent Expertise Without CRO Bias
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Because my reputation is built one study at a time, I’m driven to deliver high-quality work on every project. You get senior-level oversight, steady communication, and a consistent partner from start to finish.
Quality You Can Count On
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Expert clinical trial monitoring designed to reduce risk and protect study integrity.
Why Choose an Independent Clinical Research Assistant
Strong sites are essential to strong studies. Because I started my career at the site level, I understand what sites need to succeed — and where common challenges slow down progress.
I offer tailored support directly to sites or on behalf of study teams: from site readiness and training to ongoing communication and issue resolution. Let’s partner to help your sites stay engaged, supported, and set up to thrive.
Empowering sites with the training and support they need to perform.
site readiness
When your team is stretched thin, you need someone who can step in quickly and support your study with clarity and experience. I work closely with clients to understand their operational needs and provide hands-on support rooted in practical problem-solving, efficiency, and compliance.
Whether you need functional support, short-term resourcing, or someone to bridge a capacity gap, I help your team scale up or down with confidence.
Clear, experienced support to keep your study on track.
Clinical operations consulting
You need reliable monitoring support that scales with your study — without layers, delays, or last-minute staffing gaps. I provide full monitoring services, fractional CRA resourcing, and rapid support based on what your team needs most.
My experience includes remote and interim monitoring, site management and training, and study management support. Wherever you are in the trial lifecycle, I help you keep your study moving with consistent, senior-level oversight.
Consistent oversight when and where you need it.
clinical monitoring solutions
Explore my services
- Medical Devices
- Pharmacological research
- Clinical trials - all phases and protocol designs
With over a decade of hands-on experience across
why partner with A Clinical Research Assistant?
Start here!
Cooper T. Taylor Consulting was born from a simple belief: clinical research teams deserve support that's as adaptable and resourceful as they need to be. I founded this company to offer something different—fractional services that meet you exactly where you are, with someone who's been in your shoes and genuinely cares about your success.
I didn't start my career in clinical research thinking I'd one day run my own consulting firm—but looking back, every step prepared me for exactly this.
My journey began at the site level, working directly with patients and research teams in the trenches of clinical trials. Those years taught me what really matters: the people behind the protocols, the challenges sites face daily, and the gap between how processes are designed and how they actually work in practice.
From there, I moved into clinical operations supporting complex trials across a diverse therapeutic portfolio from cardiovascular and neuroscience to wound care and oncology. This breadth across therapeutic areas wasn't just about building expertise—it shaped how I think. It made me flexible, adaptable, and deeply convinced that there's no one-size-fits-all solution in clinical research.
What I discovered along the way is that I have a knack for seeing what others miss: the friction points that slow teams down, the process gaps that burden sites, and the opportunities to work smarter instead of harder. I'm energized by the puzzle of making complex systems work better.
Meet Andrea Taylor
founder
& principal consultant
Quality and Compliance
Site Relationship Management
Process Optimization
Monitoring Services
Clinical Trial Management
Study Management Support
specialties
case studies
Multi-center Phase III randomized controlled trial evaluating treatment efficacy and safety
A mid-sized CRO inherited a Phase III study facing mounting operational problems. Multiple monitor transitions had strained site relationships, data backlogs were growing, and sponsor confidence was slipping. The study needed immediate stabilization and experienced oversight to get back on track.
challenge
- Repeated monitor turnover causing site frustration
- Significant backlog of unresolved data queries
- Ongoing quality and compliance concerns
- Poor project management and declining sponsor trust
- Sites feeling unsupported and unheard
Specific issues
Solution & Implementation
I stepped in to rapidly stabilize the study, re-engage sites, and create clear systems for progress.
Established direct, consistent site communication to rebuild trust
Prioritized and closed outstanding queries within the first two weeks
Assessed quality issues and initiated corrective actions
Implemented structured monitoring tools to increase transparency and accountability
Improved sponsor communication and supported a smooth transition when operations later moved in-house
Strategic Monitoring Solutions
Strategic Monitoring Solutions
Strategic Monitoring Solutions
Strategic Monitoring Solutions
Strategic Monitoring Solutions
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templates for your clinical research
I believe the best templates come from real understanding. That's why I created these resources—to help you stay on top of billable hours or manage subject visits with ease. Each template is designed with the details that matter, so you can focus on your work instead of wrestling with spreadsheets. When you use these tools, you're getting more than a download—you're getting solutions to make your workflow smoother.
Ready to uplevel your processes using some of my customizable templates?
Invoice allocation Tracker & PTO Planner
Clinical Trial Subject Visit Tracker
$47
$37
Time Tracking & Invoice System
$47
Your Guide to Fractional CRA and Monitoring Support
Frequently asked questions
Getting started is simple. You can use the contact form to share your study overview, timeline, and support needs. I’ll review your project details and respond with recommended next steps for monitoring services, fractional CRA support, or broader clinical operations assistance.
How do I get started or share details about my project?
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Yes. In addition to monitoring, I support clinical operations, site management, and study management tasks such as site startup assistance, documentation tracking, vendor management, query management support, and coordination between sponsors and study team.
Can you help with clinical operations, project management, site management, or study management?
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I offer full-service monitoring from site activation to site closure. Monitoring activities include but are not limited to on-site and remote monitoring, source data verification, regulatory review, visit report writing, risk-based monitoring, and site communication. These monitoring services can be provided on a fractional, per-visit, project, or long-term basis depending on your study needs.
Can you help with clinical operations, project management, site management, or study management?
3
An independent or contract CRA (may also see it as independent CRA consultant) is a self-employed professional working on a project basis, while a fractional CRA is a specialized independent contractor who works part-time for multiple clients. A W-2 CRA (headcount) is a traditional employee who receives benefits and has taxes withheld by the employer. The primary differences are in the level of control, benefits, tax handling, and commitment.
What is the difference between independent cra vs contract cra vs fractional cra?
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A Clinical Research Associate (CRA) oversees the monitoring of clinical trials to ensure accuracy, regulatory compliance, and high-quality data. I provide expert support across all phases of clinical research, including protocol adherence, study documentation, and communication with study sites.
What is a CRA?
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