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Redcap Data Analyst Jobs in Gilbert, AZ (NOW HIRING)

Redcap Data Analyst information

See Gilbert, AZ salary details

$33.9K

$82.4K

$135.6K

How much do redcap data analyst jobs pay per year?

As of Aug 10, 2026, the average yearly pay for redcap data analyst in Gilbert, AZ is $82,376.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,300.00 and $96,700.00 per year, depending on experience, location, and employer.

How does a Redcap Data analyst typically collaborate with research teams during a clinical study?

A Redcap Data Analyst works closely with research coordinators, principal investigators, and biostatisticians to design, implement, and manage data collection instruments within the REDCap platform. They provide technical guidance on data structure, ensure data integrity, and troubleshoot issues as they arise. Regular meetings and clear communication are essential, as analysts translate research needs into database solutions and help interpret data outputs for accurate reporting. This collaborative environment supports high-quality research and facilitates smooth project workflows.

What is the difference between Redcap Data Analyst vs Clinical Data Coordinator?

AspectRedcap Data AnalystClinical Data Coordinator
Required CredentialsBachelor's in health informatics, data science, or related field; experience with REDCapBachelor's in health sciences, nursing, or related; experience with clinical data management
Work EnvironmentResearch institutions, healthcare organizations, academic settingsHospitals, clinics, research sites
Employer & Industry UsagePrimarily research-focused, data analysis, database managementClinical trial support, patient data management, regulatory compliance

Both roles involve managing health data, often using REDCap, but the Redcap Data Analyst focuses more on data analysis and reporting, while the Clinical Data Coordinator handles data collection and quality in clinical settings.

What is a Redcap Data analyst?

A Redcap Data Analyst is a professional who specializes in managing, analyzing, and reporting data collected using the REDCap (Research Electronic Data Capture) platform. They are responsible for designing data collection instruments, ensuring data quality, and performing statistical analyses to support research projects. Redcap Data Analysts often collaborate with researchers, clinicians, and IT teams to streamline data workflows and provide actionable insights from research data. Their expertise ensures that data is accurately captured, securely stored, and effectively analyzed for research purposes.

What are the key skills and qualifications needed to thrive as a Redcap Data analyst, and why are they important?

To thrive as a Redcap Data Analyst, you need strong analytical skills, experience with data management, and a background in statistics or related fields, often supported by a relevant degree. Proficiency with REDCap software, database query tools like SQL, and familiarity with data visualization or statistical analysis programs such as R or Python are typically required. Attention to detail, problem-solving abilities, and effective communication are essential soft skills for interpreting data and collaborating with research teams. These competencies ensure accurate data collection and analysis, supporting reliable research outcomes and informed decision-making.
What cities near Gilbert, AZ are hiring for Redcap Data Analyst jobs? Cities near Gilbert, AZ with the most Redcap Data Analyst job openings:
Infographic showing various Redcap Data Analyst job openings in Gilbert, AZ as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $82,376 per year, or $39.6 per hour.

Clinical Research Coordinator

Arizona Cancer Care Center

Phoenix, AZ โ€ข On-site

$22 - $29.50/hr

Full-time

Re-posted 27 days ago


Job description

Job Summary
The Clinical Research Coordinator (CRC) plays a pivotal role in the execution and management of clinical trials and research studies, working closely with principal investigators, research teams, and participants. This position ensures that all processes comply with regulatory, ethical, and organizational standards while contributing directly to the advancement of medical knowledge and patient care.
Duties and responsibilities
  • Collaborates with the Clinical Program Manager and physicians to identify, develop, organize, and implement clinical research activities.
  • Partners with principal investigators and clinical staff to plan and execute research protocols in compliance with IRB, FDA, and GCP guidelines.
  • Maintains data integrity and assists in the development of databases for effective data collection and analysis.
  • Oversee proper storage and accountability of investigational products in accordance with study protocols.
  • Ensures compliance with all research policies, protocols, and participant protection standards.
  • Conducts patient recruitment, screening, consenting, and enrollment in compliance with protocol requirements and ethical standards.
  • Coordinates study visits and procedures, ensuring protocol-specific assessments are scheduled and completed on time.
  • Tracks and reports adverse events and protocol deviations per regulatory guidelines and sponsor requirements.
  • Maintains and updates study records in regulatory binders and clinical trial management systems (CTMS), if applicable.
  • Demonstrates strict confidentiality and discretion in all matters related to research studies and participants.
  • Apply privacy and safety standards related to job responsibilities and research operations.
  • Performs other duties as assigned.

Working conditions
  • Works in an office or clinical setting.
  • Exposed to moderate noise levels.
  • Emphasizes collaboration with various stakeholders.
  • Necessitates effective communication and teamwork.
  • Functions in a fast-paced environment.
  • May require flexibility in working hours.
  • Requires adherence to safety protocols and compliance with healthcare regulations.
  • Valid driver's license and reliable transportation for travel between locations.

Physical requirements
  • Must be able to lift 25 lbs.
  • Must be able to sit, stand and walk for extended periods of time
  • Must be able to bend, kneel, crawl and twist as needed
  • Must be able to see, hear, type, and speak
  • Must be able to reach and pull

Qualifications/Education Requirements
  • Minimum of 2-3 years of clinical research experience required.
  • Associate or bachelor's degree in biological science, healthcare, or related medical/scientific field preferred.
  • An equivalent combination of education and relevant experience may be considered.
  • Experience with electronic data capture systems (e.g., Redcap, Medidata Rave) preferred.
  • Ability to critically evaluate information and apply problem-solving within healthcare and research settings.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Strong command of medical terminology and effective oral and written communication skills.
  • Ability to read, write, and communicate effectively in English.