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Clinical Study Associate information

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$11

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$51

How much do clinical study associate jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for clinical study associate in Arizona is $29.39, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $38.75 per hour, depending on experience, location, and employer.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Arizona? The most popular types of Clinical Study jobs in Arizona are:
What are popular job titles related to Clinical Study Associate jobs in Arizona? For Clinical Study Associate jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Clinical Study Associate jobs in Arizona look for? The top searched job categories for Clinical Study Associate jobs in Arizona are:
What cities in Arizona are hiring for Clinical Study Associate jobs? Cities in Arizona with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Arizona as of June 2026, with employment types broken down into 1% As Needed, 83% Full Time, 5% Part Time, 1% Temporary, and 10% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $61,135 per year, or $29.4 per hour.

Clinical Research Coordinator I

ALLIANCE CLINICAL LLC

Phoenix, AZ • On-site

$24 - $32/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 28 days ago

Job description

About the Role:

The Clinical Research Coordinator supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants and plays a key part in maintaining study integrity and quality.

Duties and Responsibilities:

  • Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
  • Administer questionnaires and monitor participant compliance with study protocols.
  • Respond to participant needs promptly and appropriately.
  • Collect and document patient medical history and health conditions.
  • Obtain and document informed consent from study participants.
  • Maintain accurate records of study drug dispensation and accountability.
  • Coordinate with laboratories to ensure timely testing and reporting.
  • Collect and assess information on concomitant medications.
  • Review and evaluate medical records for protocol compliance.
  • Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).
  • Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
  • Review and evaluate clinical laboratory reports.
  • Maintain up-to-date regulatory files for the research site.
  • Verify the accuracy and completeness of collected data.
  • Monitor and document temperatures for investigational product (IP) storage.
  • Support recruitment and engagement of study participants as needed.
  • Develop electronic source (e-source) documents in accordance with study protocols.
  • Manage study startup documentation, training, and timelines for assigned protocols.
  • Ensure all protocol requirements and deadlines are met consistently.
  • Adhere to all company policies, procedures, and code of conduct.
  • Maintain strict confidentiality and compliance with regulatory standards.

Qualifications:

  • At least 1 year of experience with phlebotomy and EKG procedures, or a Medical Assistant certification
  • Associate’s degree in healthcare or a related field, or equivalent relevant experience
  • 2+ years of experience in a healthcare setting
  • 2+ years of experience with FDA regulations and Good Clinical Practice (GCP)
  • Demonstrated analytical reasoning skills
  • Exceptional attention to detail and strong organizational skills
  • Excellent verbal and written communication abilities
  • Proven customer service skills with both internal and external stakeholders
  • Ability to effectively manage multiple priorities in a fast-paced environment

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.

Benefits: Medical, Dental, Vision, 401k, PTO and more!

Location: Monday – Friday / on-site / Phoenix, AZ

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.