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Edc Jobs in Arizona (NOW HIRING)

Maricopa

Courtroom Assistant - Classified

Phoenix, AZ · On-site

$27.88 - $34.50/hr

The position is currently open in Early Disposition Court (EDC) which consists of 5 high volume pretrial calendars designed for cases to be resolved quickly by taking a plea from the state or ...

ECN Operating LLC

Clinical Research Coordinator

Scottsdale, AZ · On-site

$24.50 - $32.50/hr

Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms). * Ability to work independently and as part of a multidisciplinary team. Preferred Qualifications:

Iterative Health

Clinical Research Coordinator I

Tucson, AZ · On-site

$23 - $30.50/hr

Familiarity with CTMS or EDC systems preferred Physical Requirements * Ability to sit, stand, and move throughout clinical and office environments for extended periods of time * Ability to lift and ...

DM Clinical

Clinical Research Coordinator I (3932)

Phoenix, AZ · On-site

$23 - $30.50/hr

Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training. * Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a ...

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How much do edc jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for edc in Arizona is $23.42, according to ZipRecruiter salary data. Most workers in this role earn between $19.04 and $26.88 per hour, depending on experience, location, and employer.

What are some common challenges faced by EDC (Electronic Data Capture) professionals in clinical research, and how can they be managed?

Professionals working with Electronic Data Capture (EDC) systems in clinical research often encounter challenges such as ensuring data accuracy, maintaining regulatory compliance, and managing system updates. These challenges can be managed by staying up-to-date with industry regulations, participating in ongoing training, and collaborating closely with clinical teams to streamline data entry processes. Regular communication with IT and data management teams is also crucial to address technical issues promptly and ensure smooth workflows.

What are the key skills and qualifications needed to thrive as an EDC (Electronic Data Capture) Specialist, and why are they important?

To thrive as an EDC Specialist, you need a solid understanding of clinical data management, data integrity principles, and experience with electronic data capture in clinical trials, often supported by a degree in life sciences or related fields. Familiarity with EDC systems like Medidata Rave or Oracle InForm, and certifications such as CDISC or GCP, are typically required. Attention to detail, problem-solving, and strong communication skills help you effectively collaborate with clinical teams and ensure high-quality data collection. These skills are crucial for accurate, compliant data management, which underpins the success of clinical research projects.

What are EDCs?

EDC stands for 'Everyday Carry.' In the context of jobs, an EDC typically refers to the essential tools, gadgets, or items that someone carries daily to be prepared for work or emergencies. This can include multitools, flashlights, pocket knives, pens, and other items tailored to the individual's profession or needs. People in security, law enforcement, medical fields, or even office environments often have different EDC items. The concept emphasizes practicality, preparedness, and efficiency in daily tasks.
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What job categories do people searching Edc jobs in Arizona look for? The top searched job categories for Edc jobs in Arizona are:
What cities in Arizona are hiring for Edc jobs? Cities in Arizona with the most Edc job openings:
Edc jobs near you
Infographic showing various Edc job openings in Arizona as of July 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $48,720 per year, or $23.4 per hour.
Clinical Research Coordinator II

Clinical Research Coordinator II

Headlands Research

Scottsdale, AZ

$24.50 - $32.50/hr

Other

Re-posted 15 days ago

Job description

Scottsdale, AZ
Headlands Research - Scottsdale
Full-time | Onsite (no opportunities for hybrid or remote)

For experienced CRCs looking for stability, collaboration, and meaningful work

If you're an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, Headlands Research - Scottsdale may be the right next step in your career.

Our Scottsdale site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research-particularly in vaccines, obesity and weight loss, and CNS trials.

About Headlands Research - Scottsdale

Headlands Research Scottsdale is a leading dedicated research center with diverse patient access located just north of the Scottsdale Airport. The Headlands Research Scottsdale team conducts trials in multiple therapeutic areas, including but not limited to CNS, Psych, Musculoskeletal, Addiction, Healthy Volunteers, etc. They are known for their integration of technology to streamline processes for their Sponsor/CRO partners and most importantly, subjects.

Why Experienced CRCs Choose Us
  • Multi-disciplinary collaboration with seasoned investigators and clinical staff
  • Strong operational support and clear SOPs
  • Exposure to complex, meaningful studies-not just high-volume turnover
  • Backing of a growing research network with resources and stability

This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision.

Responsibilities:

  • Provide the highest level of care for study patients
  • Deliver excellent customer service to pharmaceutical clients
  • Coordinate all aspects of assigned clinical trials from site initiation through close-out
  • Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards
  • Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
  • Manage subject recruitment, informed consent, and retention activities
  • Ensure timely EDC data entry and resolution of queries
  • Report and follow up on AEs, SAEs, and protocol deviations
  • Collaborate with investigators, sponsors/CROs, labs, and internal teams
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure training compliance for amendments and systems
  • Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
  • Mentor and coach site staff in order to further enhance quality and to best serve our volunteers

Requirements:

  • At least 4-5 years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required
  • Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required.
  • Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
  • Experience with EDC, IVRS, and clinical research platforms
  • Proficiency in medical terminology and clinical documentation
  • Strong organizational skills with the ability to manage multiple studies
  • Clear, professional verbal and written communication skills
  • Comfortable working onsite in a collaborative, clinical environment
Who Thrives in This Role
  • CRCs who want structure, support, and accountability
  • Those interested in taking the next step in managing people
  • Professionals who value teamwork over silos
  • Coordinators who care about data quality, patient experience, and compliance
  • Those ready to grow within a stable, well-established research site

 Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.

Apply