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Ccrp Jobs in Arizona (NOW HIRING)

Tucson Medical Center

Accountant Senior - Research

Tucson, AZ · On-site

$70K - $87K/yr

None required. * CPA, CMA, CGFM, or Certified Clinical Research Professional (CCRP) certification preferred KNOWLEDGE, SKILLS, AND ABILITIES : • Expert skills in excel. • Strong knowledge of ERP ...

Endeavor Health

$24.86 - $37.29/hr

Licenses: CCRP/ACRP certification or SRA International/NCURA certificate (or similar) preferred, as appropriate to the specific role. * Experience: 1-3 years of research experience with strong ...

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Ccrp information

See Arizona salary details

$20.5K

$51.1K

$75K

How much do ccrp jobs pay per year?

As of Sep 1, 2026, the average yearly pay for ccrp in Arizona is $51,117.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $58,200.00 per year, depending on experience, location, and employer.

What is a ccrp?

CCRP stands for Certified Clinical Research Professional. These professionals are credentialed by the Society of Clinical Research Associates (SOCRA) after meeting specific education and experience requirements and passing a certification exam. CCRPs play a vital role in clinical research by ensuring that studies are conducted ethically, safely, and in compliance with regulatory standards. Their responsibilities often include managing clinical trials, adhering to protocols, and maintaining high-quality data collection. Becoming a CCRP demonstrates expertise and commitment to excellence in the field of clinical research.

What are the key skills and qualifications needed to thrive as a clinical research professional (CCRP)?

To thrive as a Clinical Research Professional (CCRP), you need a solid understanding of clinical trial protocols, regulatory compliance, and data management, typically backed by a degree in life sciences and CCRP certification. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory submission platforms is essential. Attention to detail, ethical judgment, and strong organizational and communication skills distinguish top performers in this role. These competencies ensure clinical trials are conducted ethically, efficiently, and in accordance with regulatory standards.

What are some common challenges faced by clinical research coordinators (CCRCs) when managing multiple clinical trials simultaneously?

Clinical Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with various study protocols, and maintaining accurate documentation. Effective time management and strong organizational skills are crucial to prioritize tasks and prevent errors. Additionally, CCRCs frequently coordinate with investigators, sponsors, and regulatory bodies, so clear communication and adaptability are key to ensuring all trials run smoothly and meet regulatory requirements.

What is the difference between Ccrp vs Clinical Research Coordinator?

AspectCcrpClinical Research Coordinator
CertificationsRequires CCRP certificationMay or may not require CCRP, often has other certifications
Work EnvironmentResearch settings, clinical trialsHospitals, clinics, research sites
Job FocusMonitoring and managing clinical research protocolsParticipant recruitment, data collection, study coordination

The CCRP (Certified Clinical Research Professional) is a certification for professionals involved in clinical research, emphasizing monitoring and compliance. A Clinical Research Coordinator (CRC) is a role that may or may not hold CCRP certification but focuses on coordinating clinical trials and managing participant interactions. While both roles work within the clinical research industry, CCRPs often have specialized certification and focus on oversight, whereas CRCs handle day-to-day trial operations.

How do you become a certified research coordinator?

To become a certified research coordinator, individuals typically need a bachelor's degree in a health-related field and relevant experience in clinical research. They can pursue certification through organizations like the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA), which require passing an exam and maintaining ongoing education. Certification demonstrates knowledge of Good Clinical Practice (GCP) and regulatory requirements essential for the role.

What are the benefits of CCRP certification?

CCRP (Certified Clinical Research Professional) certification demonstrates a professional's knowledge and competence in clinical research, which can enhance job prospects, credibility, and earning potential. It also signifies adherence to industry standards and may be required or preferred by employers for roles involving clinical trial management and regulatory compliance.

What are popular job titles related to Ccrp jobs in Arizona?

For Ccrp jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Ccrp jobs in Arizona look for?

The top searched job categories for Ccrp jobs in Arizona are:

Ccrp jobs near you
Infographic showing various Ccrp job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 7% Part Time, and 2% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $51,117 per year, or $24.6 per hour.

Analyst II - Clinical Trials Operations

Honorhealth

Phoenix, AZ • Hybrid

$93K - $109K/yr

Full-time

Posted 25 days ago

HonorHealth rating

7.8

Company rating: 7.8 out of 10

Based on 210 frontline employees who took The Breakroom Quiz

134th of 898 rated healthcare providers

Job description

Primary City/State:

Deer Valley - 2502 W Utopia Rd Phoenix, AZ 85027

Category:

Research Operations

Shift:

Day

Department:

HRI-Business Services ABC&E

Hybrid

Must reside in Arizona

Great care starts with great people. (Like you.)

At HonorHealth, you'll find something special. From humble beginnings in 1927 to one of Arizona's largest nonprofit healthcare systems, our culture is built on warmth and neighborly kindness. Behind every smile is a highly skilled professional with deep expertise and an unwavering dedication to what matters most - caring for the health and well-being of people and communities across the greater Phoenix area.

Responsibilities:

JOB SUMMARY

The Clinical Trial Operations Specialist II independently manages a portfolio of clinical research studies through the start-up and activation phases, ensuring accuracy, compliance and timely greenlight. This role builds and maintains study records in CTMS/EMR systems, performs detailed quality reviews, and partners with investigators and stakeholders to resolve operational issues. Specialist II provides clear reporting on study progress, timelines, and barriers, preparing updates and presentations for leadership as needed. By exercising full ownership of assigned studies, this role ensures seamless progression through the Clinical Trial Business Operations workflow while mentoring junior staff.

ESSENTIAL FUNCTIONS
  • Portfolio ManagementIndependently oversee assigned clinical trials through start-up and activation.Ensure accuracy, compliance, and timely completion of deliverables.
  • Build & Review Study RecordsCreate and maintain CTMS and EMR study builds with minimal oversightPerform detailed quality reviews to identify and resolve discrepancies
  • Own Study Progress & ReportingServe as primary owner of assigned studies within the CTBO workflow.Provide regular updates on timelines, barriers, and progress.Prepare and deliver study status presentations for leadership
  • Mentor & CollaborateSupport training of junior staff through knowledge sharing.Partner with investigators and stakeholders to resolve operational issues.
  • Performs other duties as assigned.

EDUCATION
  • High School Diploma or 4 years of relevant experience Required or
  • Associates or 2 years of relevant experience Required
  • Bachelors in Healthcare, Science, Business, or related discipline Preferred

EXPERIENCE
  • , Experience in Clinical Research Operations, with demonstrated competency in CTMS/EMR builds, study start-up, or research business operations 2 years Required
  • , Experience independently managing study start-up activities, conducting quality reviews, and preparing status reports for leadership Preferred

LICENSE AND CERTIFICATIONS
  • Certification in clinical research (e.g., ACRP-CP, CCRC, CCRP) Preferred

We're all in for your career.

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About HonorHealth

Sourced by ZipRecruiter

HonorHealth is a non-profit, local community healthcare system serving an area of 1.6 million people in the greater Phoenix area. The network encompasses six acute-care hospitals, an extensive medical group, outpatient surgery centers, a cancer care network, clinical research, medical education, a foundation, and community services with approximately 13,100 team members, 3,500 affiliated providers and nearly 700 volunteers. HonorHealth was formed by a merger between Scottsdale Healthcare and John C. Lincoln Health Network. HonorHealth's mission is to improve the health and well-being of those we serve.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Scottsdale, AZ, US

Year founded

2014

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