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Clinical Trials Associate Jobs in Arizona (NOW HIRING)

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Clinical Research Associate

Phoenix, AZ

Clinical Research Associate - Oncology - Phoenix ICON is a global healthcare intelligence and ... Experienced monitoring Oncology (Prostate Cancer, and Lung Cancer) and HemeONC clinical trials.

ICON

Clinical Research Associate

Phoenix, AZ · On-site +1

Clinical Research Associate - Oncology - Phoenix ICON is a global healthcare intelligence and ... Experienced monitoring Oncology (Prostate Cancer, and Lung Cancer) and HemeONC clinical trials.

Banner Health

IBD BUMCP POS13715

Phoenix, AZ · On-site

$86K - $119K/yr

Eligibility for appointment at the Assistant/Associate Professor level. Preferred Qualifications: * Experience leading clinical trials or translational research programs. * Record of securing ...

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How much do clinical trials associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trials associate in Arizona is $37.26, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $41.01 per hour, depending on experience, location, and employer.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

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

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

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

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

What are the most commonly searched types of Clinical Trials jobs in Arizona?

The most popular types of Clinical Trials jobs in Arizona are:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Arizona as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $77,504 per year, or $37.3 per hour.

Board-Certified Hematologist/Oncologists

American Society of Clinical Oncology (ASCO)

Phoenix, AZ • On-site

$250/hr

Other

Posted 8 days ago

Job description

Ironwood Physicians, PCis an independent private practice, and the largest cancer provider in the metro Phoenix market. We are a multi-disciplinary physician-centric and collaborative group located across 15 sites throughout the greater Phoenix area. Our well diversified practice provides medical oncology, radiation oncology, gynecologic oncology, breast surgery, diagnostics (PET/CT), clinical research trials, and urology services.

Our state-of-the-art-centers are patient focused and possess the highest quality equipment allowing us to conveniently deliver care in an integrated setting.

In addition to our satellite offices, our 6 comprehensive cancer centers support 45 medical oncologists, 11 radiation oncologists, 13 breast surgeons and 2 gynecologic oncologists. Located throughout the beautiful Valley of the Sun, there is a full cadre of healthcare support facilities, excellent consultants, a friendly community and dedicated, well–trained associates.

We have created six oncology sub-divisions to keep abreast of the latest evolving treatments so we may continue to provide academic level cancer care in our community setting. In addition to their specialized practice, all of our medical oncologists continue to see hospital and benign hematology patients in the outpatient setting as is consistent with community practice.

Ironwood Cancer & Research Centers (Ironwood Physicians, PC)is now seeking highly trained board-certified Hematologist/Oncologists for ourBreast, Lung,andGenitourinarydivisions. Candidates must be fellows or junior faculty and will have a chance to participate in our robust clinical trials program with an opportunity to be published.

Candidates must possess superior clinical communication skills, a team mentality, and demonstrate the ability to develop interdisciplinary collaborations. This exclusive opportunity includes a highly competitive financial package.

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