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Clinical Research Associate Jobs in Gilbert, AZ (NOW HIRING)

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 - 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 ...

DescriptionPosition Summary The Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials conducted at CND's Clinical Research Center site and investigator sites ...

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Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential ...

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential ...

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Clinical Research Associate information

See Gilbert, AZ salary details

$11

$40

$69

How much do clinical research associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical research associate in Gilbert, AZ is $40.99, according to ZipRecruiter salary data. Most workers in this role earn between $28.75 and $52.50 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Gilbert, AZ?

The most popular types of Clinical Research jobs in Gilbert, AZ are:

What cities near Gilbert, AZ are hiring for Clinical Research Associate jobs?

Cities near Gilbert, AZ with the most Clinical Research Associate job openings:

Infographic showing various Clinical Research Associate job openings in Gilbert, AZ as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $85,269 per year, or $41 per hour.

Clinical Research Associate

St Joseph Hospital & Medical Center

Phoenix, AZ โ€ข On-site

$35.62 - $52.99/hr

Full-time

Re-posted 5 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 worldโ€™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.ย 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 experienceย 
  • 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 Josephโ€™s Hospital and Medical Center (SJHMC)ย 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.


Qualifications:

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 experienceย 
  • Experience with Microsoft Office Suite Systems

Preferred

  • Registered Nurse: AZ
  • Physical Therapist: AZ
  • Occupational Therapist: AZ and
  • Clinical Research Associate
  • Certified Clinical Research Professional
Employment Type: Full Time