Skip to main content
Tallo logoTallo logo

Clinical Research Coordinator-Founding Role

Job

CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC.

Winter Park, FL (In Person)

Full-Time

Posted 6 weeks ago (Updated 5 weeks ago) • Actively hiring

Expires 5/28/2026

Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
83
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

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 (MRI, Neurosurgery, Orthopedics, and Pain Management) launching a dedicated Clinical Research Division. We are seeking a powerhouse Clinical Research Coordinator (CRC) to serve as our founding lead. You will be the architect of our research infrastructure, working directly with our Board-Certified Physicians to transition our clinical excellence into a world-class investigative site.
Core Responsibilities Division Launch:
Develop and implement Standard Operating Procedures (SOPs) for study conduct, drug/device storage, and data management.
Study Startup:
Lead the feasibility process, attend Site Selection Visits (SSVs), and manage the regulatory "green light" process (IRB submissions, 1572s, CVs, and Training Logs).
Patient Management:
Oversee the entire "subject" lifecycle, from pre-screening our existing patient database to Informed Consent, randomization, and follow-up visits.
Sponsor Relations:
Act as the primary point of contact for CROs and Sponsors; host Monitoring Visits (CRAs) and ensure 100% "inspection-ready" source documentation.
Quality Assurance:
Maintain ALCOA+ standards for all data entry in EDC systems and manage SAE (Serious Adverse Event) reporting with the Principal Investigator.
Qualifications & Requirements Experience:
Minimum of 5+ years of active clinical research experience. Experience in Surgical, Orthopedic, Pain management or Device trials is highly preferred.
Certification:
CCRC (ACRP) or CCRA (SOCRA) certification is required.
Technical Skills:
Deep familiarity with GCP/ICH guidelines and experience with multiple EDC platforms (e.g., Medidata Rave, Veeva, Oracle).
Leadership:
Proven ability to work independently. You must be comfortable telling a Surgeon what they need to sign and when.
Education:
Bachelor's degree in Life Sciences, RN, or equivalent clinical background. Why Join Us?
Build Your Legacy:
You will have the autonomy to build this division your way, with full support from ownership and access to state-of-the-art MRI and surgical facilities.
Competitive Compensation:
Salary commensurate with experience.
Growth:
As the division grows, this role is positioned to evolve into a Director of Research position. Background Screening (Florida): This position requires Level 2 screening through the Florida Care Provider Background Screening Clearinghouse.
Learn more:
https://info.flclearinghouse.com

Similar jobs in Winter Park, FL

Similar jobs in Florida