Clinical Research Coordinator III – Thunderbird Office

Insperity; Phoenix (AZ); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Competitive salary

Paid time off

Medical benefits

Dental benefits

Vision benefits

Growth opportunities

Job summary

A healthcare center in Arizona is seeking an experienced Clinical Research Coordinator III. The ideal candidate will lead complex clinical trials, mentoring junior staff while ensuring adherence to protocols and regulatory standards. Strong patient care, leadership, and organizational skills are essential. Join a collaborative team that values growth and success in clinical research.

Qualifications

• Minimum 3+ years of clinical research experience with demonstrated ability to lead trials.
• Experience training and mentoring junior team members.
• Bilingual proficiency is considered a strong asset, though not required.

Responsibilities

• Independently coordinates all phases of multiple clinical trials.
• Mentors junior coordinators and ensures compliance with protocols.
• Educates patients on study requirements and assists in clinical visits.
• Mentor CRC I/II staff and provide protocol guidance.
• Lead in-services and contribute to audits and training.

Skills

Patient care skills

Medical knowledge application

Communication skills

Leadership and mentorship

Organizational skills

Proficient in regulatory and clinical software

Problem-solving ability

Clinical trial operations

Organizational & data management

Education

Bachelor’s degree in life sciences, nursing, or related field

Clinical Research Coordinator Certification (e.g., ACRP, SOCRA)

Tools

EDC

CTMS

IRT

Clinical software

Job description

Clinical Research Coordinator III – Thunderbird Office

Arizona Kidney Disease and Hypertension Center (AKDHC) is one of the nation’s largest groups of physicians specializing in the care of patients with renal disease. Since 1976, we have enjoyed the trust of patients and the respect of the community throughout the Phoenix Metropolitan area and across Arizona. We are a professional medical association consisting of physicians and other vital support staff. We are seeking a Clinical Research Coordinator III to join our team. To learn more about us, please visit our website: www.akdhc.com .

The Clinical Research Coordinator III is a senior-level coordinator responsible for executing multiple complex clinical trials from site initiation to close-out. Under the guidance of the Clinical Research Operations Manager, this role serves as a subject matter expert in protocol management, sponsor relations, and regulatory compliance. The CRC III mentors junior coordinators support internal audits and provides training and oversight to ensure protocol fidelity and operational excellence. This position requires strong clinical knowledge, leadership, and the ability to work independently across multiple research sites.

Essential Functions

• Advanced Trial Coordination & Oversight
  • Independently coordinates all phases of multiple clinical trials simultaneously across various stages and locations.
  • Ensures study procedures comply strictly with protocol, GCP, and regulatory requirements.
  • Travels between study sites to support patient visits, conduct in-services, and facilitate sponsor visits.
  • Represent AKDHC at sponsor Investigator Meetings and training sessions, including out-of-state travel.
• Acts as a lead coordinator and mentor to CRC I and II staff, providing hands‑on training and protocol guidance.
• Serve as back‑up to the Clinical Research Operations Manager when needed.
• Leads in‑services and ongoing education for clinical staff and providers.
• Regulatory & Quality Oversight
  • Applies deep understanding of FDA CFR, ICH‑GCP, and internal SOPs in daily trial conduct.
  • Assists in the development and execution of internal audits and in‑house monitoring activities.
  • Maintains audit‑ready study binders, data integrity, and proactive resolution of protocol deviations.
• Patient Engagement & Clinical Support
  • Educates patients on study requirements, kidney disease, dialysis, and the importance of research participation.
  • Conducts visits involving ECGs, vitals, specimen collection, phlebotomy, and medication administration under PI oversight.
  • Monitors for and reports adverse events per protocol and site SOP.

Skills Required

• Excellent patient care skills
• Demonstrated application of medical knowledge and ability to understand and comply with protocol demands
• Positive work ethic & attitude
• Excellent communication skills (both written and verbal)
• Detail‑oriented and problem‑solving ability
• Ability to work with a team and handle multiple projects
• Ability to meet deadlines and multi‑task without compromising quality
• Advanced knowledge of clinical trial operations and therapeutic area experience
• Strong leadership, mentorship, and training abilities
• Excellent organizational, data management, and documentation skills
• Ability to manage competing deadlines and lead multiple trials with minimal oversight
• Proficient in regulatory, EDC, CTMS, IRT, and clinical software
• Strong verbal and written communication, with demonstrated problem‑solving skills

Job Specifications/Requirements

• Bachelor’s degree in life sciences, nursing, or related field required (or equivalent work experience)
• Clinical Research Coordinator Certification (e.g., ACRP, SOCRA) required
• Minimum 3+ years of clinical research experience with demonstrated ability to lead trials
• Experience training and mentoring junior team members
• Bilingual proficiency is considered a strong asset, though not required

Benefits

We value our employees’ time and efforts. Our commitment to your success is enhanced by our competitive compensation and extensive benefits package including paid time off, medical, dental and vision benefits, and future growth opportunities within the company. Plus, we work to maintain the best possible environment for our employees where people can learn and grow with the company. We strive to provide a collaborative, creative environment where each person feels encouraged to contribute to our processes, decisions, planning, and culture.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.