Clinical Research Coordinator-Central Florida

Job Description

Job Description

Clinical Research Coordinator (Site Lead / Founding Role)

Location: Central Florida (On-Site)
Specialties: Neurosurgery, Orthopedics, Pain Management & Imaging
Employment Type: Full-Time

The Opportunity

We are an established, high-volume multi-specialty surgical and diagnostic practice launching a dedicated Clinical Research Division. We are seeking a powerhouse  Clinical Research Coordinator (CRC) to serve as our founding site lead.

This is  not a traditional CRC position.

We are specifically seeking an experienced research professional who understands not only how to successfully run clinical trials, but  how to identify, pursue, negotiate, and bring new clinical trials into a research site.

You will be the architect of our research infrastructure, working directly with our Board-Certified Physicians and ownership to build a premier investigative site.

A major focus of this position will be developing relationships with Sponsors and CROs, identifying study opportunities, completing feasibility and site-selection processes, securing new trials, and negotiating competitive study budgets and site terms.

Core Responsibilities

•  Study Acquisition & Business Development: Proactively identify and pursue new clinical trial opportunities with Sponsors, CROs, pharmaceutical, biotech, and medical device companies. Develop relationships with decision-makers and help position our site for study selection.

•  Sponsor & CRO Negotiations: Work directly with Sponsors and CROs to  negotiate study budgets, start-up fees, per-patient payments, screen failures, pass-through expenses, and other site-related costs and terms.

•  Feasibility & Site Selection: Lead feasibility questionnaires, qualification calls, Site Selection Visits (SSVs), and capability presentations with the goal of  converting opportunities into awarded clinical trials.

•  Division Launch: Develop and implement Standard Operating Procedures (SOPs) for study conduct, drug/device storage, regulatory compliance, and data management.

•  Study Startup: Manage the regulatory "green light" process, including IRB submissions, 1572s, CVs, training logs, essential documents, and Site Initiation Visits.

•  Patient Management: Oversee the entire subject lifecycle—from pre-screening our existing patient population through Informed Consent, randomization, study visits, and follow-up.

•  Sponsor Relations: Serve as the primary point of contact for Sponsors, CROs, and CRAs; coordinate Monitoring Visits and maintain inspection-ready documentation.

•  Quality Assurance: Maintain ALCOA+ standards for EDC and source documentation and coordinate SAE reporting with the Principal Investigator.

Dedicated CRC Support

You will  not be expected to build and operate the division alone.

This position will have a  dedicated Assistant CRC to support patient scheduling, study visits, documentation, regulatory activities, data entry, and other day-to-day research responsibilities.

This support is designed to allow the Site Lead to dedicate meaningful time to  securing new trials, Sponsor/CRO relationships, negotiations, study start-up, and overall research growth.

Qualifications & Requirements

•  Experience: Minimum 5+ years of active clinical research experience.

•  Study Acquisition Experience: Proven experience identifying, pursuing, and successfully securing clinical trials for a research site is strongly preferred and will be a major consideration in candidate selection.

•  Sponsor/CRO Experience: Demonstrated experience working directly with Sponsors and CROs on feasibility, site selection, study acquisition, and  budget negotiations.

• Experience in  Surgical, Orthopedic, Pain Management, Spine, or Medical Device trials is highly preferred.

•  Certification: CCRC (ACRP) or CCRP/CCRA or comparable research certification preferred.

•  Technical Skills: Strong knowledge of GCP/ICH guidelines and experience with major EDC platforms such as Medidata Rave, Veeva, or Oracle.

•  Leadership: Proven ability to work independently, take ownership, and confidently coordinate with physicians and executive leadership.

•  Education: Bachelor's degree in Life Sciences, RN, or equivalent clinical/research background preferred.

Why Join Us?

Build Something Significant: This is an opportunity to help build a clinical research division from the ground up—with the infrastructure already behind you.

Our organization provides access to:

• 75,000+ existing patients
• 13 affiliated medical clinics
• Board-Certified Neurosurgeons, Orthopedic Surgeons & Pain Management Physicians
• In-house MRI capabilities
• C-Arm procedure suites and diagnostic imaging
• Established clinical and patient recruitment infrastructure
•  Dedicated Assistant CRC support

We already have the  patients, physicians, facilities, and infrastructure.

We are looking for someone who knows how to turn those capabilities into  awarded clinical trials.

Career Growth: As the division expands, this position is designed to evolve into a  Director of Clinical Research  leadership role.

Competitive Compensation: Salary commensurate with experience.

We Especially Want to Hear From You If:

You can confidently say:

“I know how to bring clinical trials into a research site.”

When applying, please specifically highlight trials you have helped secure, your experience developing Sponsor/CRO relationships, and your experience  negotiating clinical trial budgets and terms.

Background Screening (Florida): This position requires Level 2 screening through the Florida Care Provider Background Screening Clearinghouse. Learn more: