ZipRecruiter

Log In

1

Clinical Research Coordinator Three Jobs (NOW HIRING)

panoramic

Clinical Research Coordinator III

Cincinnati, OH

$23.25 - $31/hr

Clinical Research Coordinator III (CRC III) Kidney & Hypertension Center Cincinnati, Ohio Advance the Future of Kidney Care Through Clinical Research Kidney & Hypertension Center is seeking an ...

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 ...

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 ...

next page

Showing results 1-20

All JobsHealthcare JobsMedical Research JobsClinical Research Manager JobsClinical Research Coordinator Three Jobs

Clinical Research Coordinator Three information

See salary details

$15

$28

$42

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

As of Aug 22, 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.
More about Clinical Research Coordinator Three jobs

What cities are hiring for Clinical Research Coordinator Three jobs?

Cities with the most Clinical Research Coordinator Three job openings:

What are the most commonly searched types of Clinical Research Three jobs?

The most popular types of Clinical Research Three jobs are:

What states have the most Clinical Research Coordinator Three jobs?

States with the most job openings for Clinical Research Coordinator Three jobs include:

What job categories do people searching Clinical Research Coordinator Three jobs look for?

The top searched job categories for Clinical Research Coordinator Three jobs are:

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 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Coordinator III

DM Clinical Research

Jersey City, NJ

$25.25 - $33.75/hr

Full-time

Re-posted 4 days ago

Job description

Clinical Research Coordinator III

The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES amp; RESPONSIBILITIES
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training, as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
  • Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
  • Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
  • Ability to train and mentor site staff, as needed
  • Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
  • Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
  • Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
  • Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings
  • Any other matters as assigned by management
KNOWLEDGE amp; EXPERIENCE
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree preferred
  • Foreign Medical Graduates preferred
Experience:
  • Minimum of 5 years experience in Clinical Research
  • Supervisory experience preferred
  • Wide therapeutic range of clinical trials experience preferred
  • Regulatory research experience is a plus
Credentials:
  • ACRP or equivalent certification is preferred
Knowledge and Skills:
  • Goals-driven while continuously maintaining quality.
  • Must be detailed-oriented, proactive, and able to take initiative.
  • Must have strong written and communication skills.
  • Must have excellent customer service skills.
  • Bilingual in Spanish is a plus

Apply