Expert Support for Clinical Research Sites

My name is Celeste Gonzalez, I’m a Clinical Research Professional with over two decades of experience guiding research sites through every phase of clinical trials — from startup to closeout.

Throughout my career, I’ve worked hands-on as a Clinical Research Coordinator (CRC), Site Manager, and Sr. Site Development Specialist- In-House CRA, giving me a well-rounded perspective of both the site and sponsor sides of research. This blend of experience allows me to understand not only what sponsors expect, but also the real-world challenges that sites and CRCs face every day.

Over the years, I’ve supported newly established research sites in building their programs from the ground up — and helped sites struggling after CRC turnover or audit findings to regain positive momentum. My work focuses on rebuilding structure, training staff, and creating efficient systems that help teams stay compliant and confident.

I know firsthand how overwhelming it can be to manage startup forms, source documentation, regulatory submissions, patient scheduling, and data entry — often with limited support. That’s why I created this consulting service: to bridge the gap between sponsor expectations and site execution, giving sites the tools and mentorship they need to thrive.

I hope to bring on other experienced CRC's as the company continues to grow.

My mission is simple: to help clinical research sites operate with confidence, quality, and efficiency, while empowering CRCs to succeed in their roles and produce exceptional data.

About your Site Support Partner
Why Choose Us

Our flexible support services include site startup, regulatory preparation, and CRC training — ensuring your research program runs efficiently and continues to grow without the expense of hiring a full-time employee for oversight and guidance.

We specialize in helping new or inexperienced CRCs gain the confidence, structure, and skills needed to produce high-quality work and meet study expectations.

From my experience, small research sites often face high turnover when CRCs feel overwhelmed by study demands or feel unsupported in their roles. Having an experienced professional to discuss challenges, plan next steps, and provide judgment-free guidance can make all the difference.

When CRCs feel supported, studies stay on track — and your site succeeds with stronger data, better compliance, and higher retention.

Doctor consulting with an elderly patient in an office.
Doctor consulting with an elderly patient in an office.

The consulting team streamlined our processes, enhancing compliance and efficiency in our research operations.

Dr. Smith

A diverse group of professionals collaborating over clinical research documents in a modern office.
A diverse group of professionals collaborating over clinical research documents in a modern office.
A close-up of hands reviewing regulatory documents with a laptop and coffee cup on the table.
A close-up of hands reviewing regulatory documents with a laptop and coffee cup on the table.

★★★★★