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Clinical Research Coordinator Three Jobs (NOW HIRING)

University of Miami

Clinical Research Coordinator 3

Miami, FL · On-site

$23.25 - $30.75/hr

Clinical Research Coordinator 3 The University of Miami/UHealth department of Neurology has an exciting opportunity for a Full Time Clinical Research Coordinator 3 to work at the UHealth Medical ...

System One

Clinical Research Coordinator III

Carnegie, PA · Remote

$24.75 - $33/hr

Clinical Research Coordinator III Location: Pittsburgh, PA, Hybrid: Combination of On-Campus or Remote determined by the department. Schedule: Varied based on participants schedule Type: Direct Hire ...

University of Miami

Clinical Research Coordinator 3

Miami, FL · On-site

$23.25 - $30.75/hr

The Clinical Research Coordinator 3 (A) serves as an experienced clinical research professional responsible for providing leadership in the planning, implementing, monitoring, and evaluating of ...

University of Miami

Clinical Research Coordinator 3

Miami, FL · On-site

$23.25 - $30.75/hr

CORE SUMMARY The Clinical Research Coordinator 3 serves as experienced clinical research professional responsible for providingleadership in the planning, implementing, monitoring, and evaluating of ...

UAB

CLINICAL RESEARCH COORDINATOR III

Tampa, FL · On-site

$60K - $98K/yr

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Coordinator III. The Clinical Research Coordinator III serves as the primary ...

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How much do clinical research coordinator three jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical research coordinator three in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What are the top 5 skills of a clinical research coordinator?

A clinical research coordinator needs strong organizational skills to manage study protocols and data, excellent communication abilities to interact with participants and staff, attention to detail for accurate data collection, knowledge of regulatory requirements and Good Clinical Practice (GCP), and proficiency with data management tools and electronic health records. These skills ensure effective study coordination and compliance with industry standards.

What is the career progression for a clinical research coordinator?

Career progression for a clinical research coordinator often involves gaining experience and additional certifications, which can lead to roles such as senior coordinator, clinical research manager, or project manager. Some may advance into clinical trial management, regulatory affairs, or move into related healthcare or research positions, often requiring strong organizational skills and knowledge of regulatory guidelines.

What other jobs can I get as a clinical research coordinator?

Clinical Research Coordinators can transition into roles such as Clinical Research Managers, Clinical Trial Managers, or Regulatory Affairs Specialists, leveraging their experience in study management, compliance, and data collection. They may also move into positions like Clinical Data Managers or Medical and Health Services Managers, often requiring additional certifications or training in project management or regulatory standards.
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Clinical Research Coordinator Three jobs near you
Infographic showing various Clinical Research Coordinator Three job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Coordinator III

Tulane University Translational Science Institute

New Orleans, LA • On-site

$70 - $90/hr

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Posted yesterday

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Job description

The primary responsibility of the Clinical Research Coordinator III is to manage all aspects of conducting clinical trials, with minimal supervision. The Clinical Research Coordinator III is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocol, the Clinical Research Coordinator III acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator III screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring, and works independently in designing, coordinating, and implementing all assigned research projects. The Clinical Research Coordinator III is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.

Responsibilities
  • Knowledge of good clinical research practice is required
  • In-depth knowledge of IRB submission process and requirements
  • Must be able to interact well with patients and the general public
  • Ability to acquire and maintain all required CITI training certificates
  • Ability to acquire and maintain credentialing at all required institutions: Tulane Medical Center, Veterans Administration Hospital/New Orleans, LA and University Medical Center
Qualifications

Minimum Qualification:

  • Bachelor’s degree or RN with current Louisiana state licensure at the time of hire and two (2) years of related work experience.
  • Or
  • LPN with current Louisiana state licensure at the time of hire and five (5) years of related work experience.
  • Or
  • Master’s degree and one (1) year of related work experience

Preferred Qualification:

  • Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP)
  • OR
  • Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired
  • Supervisory experience is preferred
About Us

Tulane University is an equal opportunity educator and employer committed to providing an education and employment environment free of unlawful discrimination, harassment, and retaliation. Legally protected demographic classifications (such as a person’s race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane’s employment or educational programs or activities.

Tulane University is responsible for providing reasonable accommodations to individuals with disabilities throughout the applicant screening process. If you need assistance in completing an application or during any phase of the interview process, please contact the Office of Human Resources by phone at 504-865-4748 or by email at hr@tulane.edu.

Job Info
  • Job Identification 1355
  • Job Category Research
  • Posting Date 07/22/2026, 07:23 PM
  • Job Schedule Full time
  • Job Shift Day
  • Locations New Orleans, LA, United States
  • Legal Employer Tulane University
  • Business Unit Tulane University
  • Department SOM Medicine - Tulane Research Innovation for Arrhythmia Discoveries (TRIAD)
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