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Clinical Research Coordinator Rheumatology Jobs (NOW HIRING)

Alcanza Clinical Research

$23.50 - $31.25/hr

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

Amicis Research Center

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Clinical Research Coordinator

Santa Clarita, CA · On-site

$25 - $40/hr

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This role is crucial in managing and overseeing clinical trials, ensuring compliance with regulatory ...

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

As of Aug 20, 2026, the average hourly pay for clinical research coordinator rheumatology 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 does a clinical research coordinator in rheumatology do?

A Clinical Research Coordinator (CRC) in Rheumatology is responsible for managing clinical trials and research studies focused on rheumatic diseases, such as arthritis and lupus. Their duties include recruiting and enrolling patients, ensuring studies comply with ethical and regulatory requirements, collecting and managing data, and coordinating with physicians and research staff. The CRC also helps with patient education, scheduling study visits, and maintaining accurate records to ensure the integrity of research data. They play a key role in advancing rheumatology treatment options through high-quality clinical research.

What are the key skills and qualifications needed to thrive as a clinical research coordinator in rheumatology?

To thrive as a Clinical Research Coordinator in Rheumatology, you need a background in life sciences or healthcare, experience in clinical trial management, and knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and certifications like ACRP or SOCRA is highly valued. Strong organizational skills, attention to detail, and effective communication are crucial for managing studies and collaborating with diverse teams. These skills ensure the integrity of research, patient safety, and compliance with complex regulatory requirements in rheumatology trials.

What are some common challenges faced by clinical research coordinators in rheumatology studies?

Clinical Research Coordinators in Rheumatology often encounter challenges such as managing complex protocols for multiple ongoing studies, ensuring patient retention over long study periods, and handling diverse data collection requirements. Coordinators must also navigate frequent communication with multidisciplinary teams, including physicians, nurses, and data managers, while keeping up with regulatory documentation. Developing strong organizational skills and building rapport with patients can help address these challenges and contribute to the success of clinical trials.

What is the difference between Clinical Research Coordinator Rheumatology vs Clinical Research Coordinator Oncology?

AspectClinical Research Coordinator RheumatologyClinical Research Coordinator Oncology
Required CredentialsBS or BA, clinical research certification preferredBS or BA, clinical research certification preferred
Work EnvironmentRheumatology clinics, hospitals, research centersOncology clinics, hospitals, research centers
Employer & Industry UsageMedical research institutions, hospitals, pharmaceutical companiesHospitals, cancer centers, pharmaceutical companies
Common Search & ComparisonYesYes

The Clinical Research Coordinator Rheumatology and Clinical Research Coordinator Oncology roles share similar credentials, work environments, and employer types. The main difference lies in the medical specialty focus: rheumatology involves autoimmune and musculoskeletal diseases, while oncology centers on cancer research. Both roles require coordination of clinical trials, patient interaction, and adherence to regulatory standards, but their specific disease focus distinguishes them.

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Clinical Research Coordinator Rheumatology jobs near you
Infographic showing various Clinical Research Coordinator Rheumatology job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Regional Manager

Arizona Arthritis & Rheumatology Associates

Rockville, MD • On-site

$96K - $106K/yr

Full-time

Posted 14 days ago

Job description

Arizona Arthritis & Rheumatology Associates, P.C. is the largest private Rheumatology practice in the United States. The practice has over 60 providers, 15 sites and over 350 employees providing assessment and treatments for our rheumatology patients. Our providers work together to keep patients healthy, and are recognized for excellence in medicine and for being pioneers in new treatments, ably supported by our Research department.
We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.
Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care.
We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Coordinator to join our team.
The Regional Research Manager reports to the Director of Clinical Research and is responsible for the clinical research staff & daily operations at each assigned medical clinic (research site).
RESPONSIBILITIES
  • Travel daily to research sites to provide support and complete job responsibilities listed below
  • First line manager (direct, supervise, and evaluate) to research coordinators and assistants
  • Conduct training and mentorship of new clinical research staff, ensuring their success
  • Assign tasks and studies to ensure workloads are balanced among recruitment staff
  • Utilize Clinical Trial Management System weekly to ensure productivity goals are met
  • Monitor electronic source data capture system reports to ensure data and query goals are met
  • Meet with employees monthly to review metrics and conduct weekly huddles with the team
  • Perform HR responsibilities including interviews, reviews, reprimands, and terminations
  • Manage operations at the clinical sites and facilitate all medical staff's participation in research
  • Implement Clinical Trial Agreements & Budgets and ensure model fiscal operations
  • Assist with qualifying and onboarding vendors and staff for clinical services as required per study
  • Approve and order supplies and equipment as needed from sponsors and vendors
  • Ensure clinical research staff have the skills and resources necessary for success
  • Ensure clinical sites have the medical equipment and resources necessary for success
  • Ensure clinical sites are engaging in recruitment activities and meeting patient enrollment goals
  • Facilitate operational changes using professional and positive motivation
  • Ensure compliance with research protocols, handbook policies, standard operating procedures, ICH-GCP Standards, FDA regulations, medical laws and implement solutions for compliance
  • Perform quality assurance and complete corrective action and prevention assessment plans
  • Conduct Pre-Study Visits and Site Initiation Visits for new clinical trials
  • Serve as an escalation point all clinical trials and first point of contact for site staff members
  • Provide ongoing support, needs assessment, and issue resolution to clinical sites and staff on an ongoing basis, and escalate to Director of Clinical Research when needed
  • Communicate with physicians, vendors, sponsors and CROs to address and resolve issues
  • Collaborate with fellow Regional Research Managers to ensure a consistent and coordinated department and management style across all sites nationally
  • Meet with administrative staff regularly to ensure all research operations are running smoothly
  • Perform duties for coordinators and managers when there is a lapse in coverage
  • Participate in continuing education to remain a subject matter expert on all research protocols, medical indications, company policies, standard operating procedures, ICH-GCP regulations, FDA 21 CFR, IRB Guidelines, and all applicable local and federal medical laws

Learn more about AARA on our website at http://azarthritis.com
Requirements
QUALIFICATIONS
  • Bachelor's Degree, or equivalent
  • 2 years' experience as clinical research coordinator
  • Subject Matter expert in clinical research and relevant clinical indications
  • Understands specific state and federal regulations governing medicine and privacy
  • Possess strong leadership & organizational skills
  • Excellent verbal and written communication skills
  • Willing and able to travel to all regional offices daily
  • Management experience and/or formal training preferred but not required
  • Clinical Research Certification (CRCC/CCRP) preferred but not required

Salary Description
96,000-106,000

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