Clinical Research Coordinator III RN Neuro

Texas Health Huguley FWS; Orlando (FL); On-site; USD 60,000 - 95,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator III RN to oversee clinical trials and ensure compliance with FDA regulations. This role involves coordinating research studies, managing timelines, and delivering safe patient care while mentoring new coordinators. The ideal candidate will thrive in a fast-paced environment, demonstrating strong assessment and communication skills. Join a dedicated team where your contributions will enhance patient care and research quality, all while enjoying a supportive community focused on professional growth.

Benefits

Benefits from Day One

Paid Days Off from Day One

Mental Health Resources and Support

Pet Insurance

Qualifications

• 2-5 years of experience in biomedical research or related fields.
• Professional certification in a research-focused clinical specialty is preferred.

Responsibilities

• Coordinates clinical research studies, managing all activities and timelines.
• Monitors and evaluates quality and safety of clinical operations.

Skills

Assessment Skills

Phlebotomy

IV Insertion

Study Coordination

Communication Skills

Detail-oriented

Critical Thinking

Organizational Skills

Adaptability

Interpersonal Skills

Education

Active Florida RN License

BLS Certification

CCRP Certification

Tools

Microsoft Office

Job description

Job Description - Clinical Research Coordinator III RN Neuro (25017344)

Job Description

Clinical Research Coordinator III RN Neuro (

Job Number:

25017344

Description

All the benefits and perks you need for you and your family:

• Benefits from Day One
• Paid Days Off from Day One
• Mental Health Resources and Support
• Pet Insurance*

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full-Time

Shift : Days

The community you’ll be caring for: Insert Marketing Statement

The role you’ll contribute:

The Clinical Research Coordinator III RN serves at AdventHealth Research Institute (AHRI), providing oversight of industry-sponsored and investigator-initiated clinical trials in accordance with protocols, FDA regulations, and ICH/GCP guidelines. Acts as a clinical study coordinator and lead for aligned clinical projects. Collaborates with AHRI teams to ensure smooth operations and actively participates in customer service and relationship maintenance.

The value you’ll bring to the team:

• Delivers safe care, respecting all participants. Maintains clinical skills including assessment, phlebotomy, IV insertion, and practices Universal Precautions. Understands HIPAA regulations.
• Maintains a clean, prepared clinical space; performs setup and turnover procedures per SOPs.
• Participates in training to maintain licensure.
• Coordinates clinical research studies, managing all activities and timelines.
• Develops and implements processes to optimize workflow and quality standards.
• Serves as preceptor and mentor for new study coordinators.
• Establishes and maintains SOPs for clinical operations and staff training.
• Leads or participates in special projects to improve research operations.
• Monitors and evaluates quality and safety of clinical operations.
• Supports safe care with dignity and respect for all patients/participants.
• Performs other duties as needed for efficient operations.

The expertise and experiences you’ll need to succeed:

• Ability to assist with procedures and study requirements within scope of practice.
• Adaptability to various clinical settings per protocol.
• Skills in assessment, phlebotomy, IV insertion, and drug administration.
• Proficiency in study coordination across trial types.
• Knowledge of FDA, CDC, DHHS regulations.
• Ability to work independently in a fast-paced environment.
• Strong interpersonal and communication skills.
• Detail-oriented, organized, motivated, and efficient under pressure.
• Ability to manage multiple trials and duties independently.
• Knowledge of patient needs in research trials, including device management.
• Critical thinking and analytical problem-solving skills.
• 2-5 years of experience in biomedical research or related fields.
• Experience with informed consent, biospecimen handling.
• Proficiency in Microsoft Office and internet skills.
• Minimum 3 years of clinical research experience.
• Specialty experience as assigned.
• Active Florida RN license, BLS, and CCRP certification (ACRP or SOCRA).

Professional certification in a research-focused clinical specialty is preferred.