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Clinical Research Associate Manager Jobs in Arizona

Your main responsibilities as a Research Associate II: · Responsible for conducting research ... Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined ...

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Clinical Research Associate - Oncology - Phoenix ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Clinical Research Associate - Oncology - Phoenix ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Clinical Research Associate II

Phoenix, AZ · On-site

$91K - $114K/yr

Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate Manager information

See Arizona salary details

$33.5K

$80.6K

$128.6K

How much do clinical research associate manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for clinical research associate manager in Arizona is $80,567.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,300.00 and $106,200.00 per year, depending on experience, location, and employer.

What is a clinical research associate manager?

A Clinical Research Associate Manager is a professional responsible for overseeing and managing a team of Clinical Research Associates (CRAs) who monitor clinical trials to ensure they are conducted according to protocols, regulatory requirements, and good clinical practice. They coordinate trial activities, provide guidance and training to CRAs, and serve as a liaison between the research team, sponsors, and regulatory bodies. Their role is crucial for maintaining the quality and integrity of clinical research studies.

What are the key skills and qualifications needed to thrive as a clinical research associate manager, and why are they important?

To thrive as a Clinical Research Associate Manager, you need expertise in clinical trial management, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and project management certifications like PMP are commonly required. Strong leadership, communication, and problem-solving skills help you effectively oversee teams and ensure adherence to protocols. These skills are crucial for ensuring high-quality research, regulatory compliance, and successful project delivery in clinical studies.

What are some common challenges faced by clinical research associate managers when overseeing multiple clinical trials simultaneously?

Clinical Research Associate Managers often face the challenge of balancing oversight across several ongoing clinical trials, each with unique protocols and site requirements. Managing competing deadlines, ensuring regulatory compliance, and maintaining clear communication across diverse teams are critical aspects of the role. Effective prioritization, strong organizational skills, and proactive risk management are essential to navigate these complexities and ensure trial success. Collaboration with CRAs, investigators, and cross-functional departments helps in addressing site issues promptly and maintaining study quality.

Is it hard to get a clinical research associate manager job?

Securing a clinical research associate manager position can be competitive, often requiring several years of experience in clinical research, strong leadership skills, and relevant certifications such as CCRP or RAC. Candidates with a background in clinical operations, good understanding of regulatory requirements, and proficiency with trial management tools tend to have better prospects.

What cities in Arizona are hiring for Clinical Research Associate Manager jobs?

Cities in Arizona with the most Clinical Research Associate Manager job openings:

Infographic showing various Clinical Research Associate Manager job openings in Arizona as of August 2026, with employment types broken down into 87% Full Time, 10% Part Time, 2% Temporary, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $80,567 per year, or $38.7 per hour.

$35.62 - $52.99/hr

Full-time

Posted 24 days ago


Job description


Job Summary and Responsibilities

As our Clinical Research Professional you will be instrumental in advancing medical knowledge by expertly managing and executing clinical trials. You will ensure the highest standards of data integrity patient safety and regulatory compliance throughout the research process.

Every day you will manage trial activities including participant recruitment data collection and documentation serving as a key liaison for all stakeholders. You will ensure strict adherence to protocols and regulatory requirements from study initiation to completion.

To be successful in this role you will bring relevant clinical research experience and a strong understanding of regulatory guidelines. Your exceptional organizational skills attention to detail and ability to communicate effectively will be crucial in this dynamic field.

At Barrow Neurological Institute (BNI) one of the world’s premier neuroscience centers we are leading groundbreaking multicenter clinical research to accelerate discoveries for people living with amyotrophic lateral sclerosis (ALS). As part of our Academic Clinical Research Organization (CRO) you will join a nationally recognized team coordinating NIH/NINDS funded studies that are changing how ALS is diagnosed monitored and ultimately treated. We are seeking a motivated Clinical Research Associate (CRA) to support field monitoring activities across a network of leading academic medical centers participating in innovative ALS clinical research studies. This role offers the opportunity to work alongside dedicated research sites while ensuring the highest standards of participant safety regulatory compliance and data quality.

Position responsibilities include:

  • Responsible for all aspects of clinical monitoring site management and trial administration as prescribed in the monitoring plan and as instructed by program leadership.
  • Employee is responsible for working with sites during study start up including assessing site feasibility as required provide ongoing training and site initiation visits conducting remote monitoring and approx. 25-30 interim onsite and closeout field monitoring visits located throughout the US and Canada. During each monitoring visit the CRA is responsible for the evaluation of clinical data documentation regulatory document review monitor safety and conduct of study to ensure investigator and site compliance with study protocol overall clinical objectives FDA regulations ICH/GCP guidelines institutional/ CRO SOPs and HIPAA guidelines.
  • The CRA is expected to work cooperatively with study team and operations management to proactively drive project success. Completes preparation and submission of accurate and timely monitoring reports and other requested deliverables as outlined in the Study Monitoring Plan or as requested by program leadership.
  • Effective long-term planning/scheduling of remote and on-site monitoring visits in accordance with the Study Monitoring Plan or as requested by program leadership.
  • Perform Lead Study Monitoring activities as assigned including acting as the primary liaison between BNI CRO and the Clinical Study Sponsor to ensure BNI CRO provides quality monitoring and site management customer services. The Lead Study Monitor will be responsible for the timely review of all monitoring deliverables conduct co-monitoring visits and mentorship of CRA team members.
  • Participates in the quality control process for assigned monitoring activities and makes contributions to improve and adapt quality control procedures including the development of internal corrective and preventative action plans if needed and align service goals with internal and external client expectations Proactively participate in program development. This includes making contributions to the overall quality improvement of clinical monitoring services as well as actively collaborating with program leadership to expand and grow the CRO's professional portfolio.
Job Requirements

Required

  • Bachelors degree or its international equivalent in clinical, science, or health related field from an accredited institution or five (5) years equivalent work experience in lieu of the degree
  • Two (2)+ years of clinical research experience 
  • Experience with Microsoft Office Suite Systems

Preferred

  • Registered Nurse: AZ
  • Physical Therapist: AZ
  • Occupational Therapist: AZ and
  • Clinical Research Associate
  • Certified Clinical Research Professional
Where You'll Work
Hello Humankindness: Join a Legacy of Healing at Saint Joseph’s Hospital and Medical Center (SJHMC) Ready to make a real difference? Join SJHMC in Phoenix AZ., a 571-bed nonprofit founded by the Sisters of Mercy over 125 years ago. We're more than a hospital; we're a global destination for life-changing care, embracing patients with humankindness.

Here, your calling will flourish. We're not just a workplace; we're a community dedicated to a mission of service.

Leaders in Specialized Care:

  • Barrow Neurological Institute (BNI): A world-renowned center for groundbreaking neurological research and innovative treatments.
  • Norton Thoracic Institute (NTI): A national leader in advanced thoracic care with pioneering surgical techniques.
  • Level I Trauma Center: One of Arizona's busiest ERs, providing immediate, comprehensive care for critically injured patients 24/7.

Why SJHMC?

  • Culture of Excellence & Well-being: We care for our people, fostering professional and personal growth.
  • Community & Collaboration: Be part of a network committed to global health and well-being.
  • Join a Legacy, Shape a Future: Over 20% of our patients travel internationally for our specialized care.

This is an invitation to join a family of dedicated professionals at the forefront of medical innovation, united by the power of humankindness.



Pay Range
$35.62 - $52.99 /hour