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Veeva Clinical Jobs in Arizona (NOW HIRING)

Valeris

Remote Field Reimbursement Manager

Phoenix, AZ · Remote

... of clinical care/medical advice. Responsibilities * Educate HCPs on Patient Support Programs ... Highly competent in a multitude of IT capabilities to support the business needs including Veeva ...

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Veeva Clinical information

What is a Veeva Clinical professional?

A Veeva Clinical professional is someone who specializes in using the Veeva Vault Clinical Suite, a cloud-based platform designed to manage clinical trial processes and data in the life sciences industry. Their responsibilities often include implementing, configuring, and supporting Veeva Vault Clinical applications such as eTMF, CTMS, and Study Startup. These professionals help organizations streamline clinical operations, ensure regulatory compliance, and improve collaboration across trial teams. Their expertise is highly valued by pharmaceutical, biotech, and contract research organizations.

What are some common challenges faced by professionals working in Veeva Clinical roles, and how can they be addressed?

Professionals in Veeva Clinical roles often encounter challenges such as adapting to frequent software updates, ensuring data integrity across multiple studies, and coordinating with cross-functional teams like clinical operations and IT. Staying current with new features and best practices is essential to maximize the platform's capabilities. Proactive communication and ongoing training can help address these challenges, as well as building strong relationships with stakeholders to streamline workflows and resolve issues efficiently.

What are the key skills and qualifications needed to thrive as a Veeva Clinical specialist?

To thrive as a Veeva Clinical Specialist, you need a solid understanding of clinical trial processes, data management, and life sciences regulations, often supported by a degree in life sciences or related fields. Familiarity with Veeva Vault Clinical Suite, electronic data capture (EDC) systems, and relevant certifications like Veeva Vault Administrator are highly valued. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and clients. These competencies ensure the optimization of clinical workflows, regulatory compliance, and successful implementation of Veeva solutions in clinical research environments.

What are popular job titles related to Veeva Clinical jobs in Arizona?

For Veeva Clinical jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Veeva Clinical jobs in Arizona look for?

The top searched job categories for Veeva Clinical jobs in Arizona are:

What cities in Arizona are hiring for Veeva Clinical jobs?

Cities in Arizona with the most Veeva Clinical job openings:

Veeva Clinical jobs near you
Infographic showing various Veeva Clinical job openings in Arizona as of July 2026, with employment types broken down into 2% As Needed, 77% Full Time, 14% Part Time, and 7% Contract. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution.

Clinical Research Systems Quality Specialist

ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES PC

Phoenix, AZ

Full-time

Re-posted 13 days ago

Job description

Description

Our providers work together to keep patients healthy and are recognized for excellence in medicine and for being pioneers in new treatments, ably supported by our Research department.

We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.

Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care.

We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Systems Quality Specialist to join our team.

Under minimal supervision, the System Quality Specialist (SQS) owns and improves the quality, integrity, and compliance readiness of clinical research electronic systems (e.g., CTMS, eSource/EDC, eRegulatory, M365, and related reporting tools). The SQS defines data quality standards and controls, manages system change control and quality validation/testing, monitors system performance using dashboards and metrics, and maintains audit-ready documentation (SOPs, training records, configuration and validation evidence). The SQS partners with cross-functional stakeholders to implement study builds and amendments, communicate system updates, ensure appropriate access controls, and drive corrective/preventive actions to prevent recurring system and data quality issues.


RESPONSIBILITIES

  • Establish and maintain system quality management practices for clinical research platforms (e.g., CTMS, eSource/EDC, eRegulatory, M365), including documentation standards, validation evidence, and release readiness criteria
  • Ensure architecture and data inputs for systems below continuously meet or exceed minimum quality standards
  • Clinical Conductor CTMS
  • Advarra eSource +EDC
  • Veeva SiteVault eReg
  • Monday Work Management
  • SharePoint Pages & Training Workflows
  • Power Query/BI Dashboards
  • in the CTMS system for both protocol and financial compliance
  • Review, finalize and approve esource and CTMs builds for all new studies and amendments
  • Ensure all systems are updated when amendments occur and announce changes to stakeholders
  • Perform routine quality inspections of system data inputs for compliance with internal policy, standard operating procedures, ICH-GCP Standards, local and FDA regulations
  • Ensure all system quality controls are in place prior to release (e.g., procedural instructions, conditional/required fields, data constraints, standardized build templates, and controlled vocabularies) to reduce downstream queries and protocol deviations
  • Perform root cause analysis for recurring system/data quality issues; lead remediation plans to prevent reoccurrence (process, training, configuration, or automation changes)
  • Maintain dashboards/metrics (e.g., query rates, missing/late data, build defect rates, timeliness KPIs) and drive corrective/preventive actions


Learn more about AARA on our website at http://azarthritis.com

Requirements

QUALIFICATIONS

  • Bachelor's Degree or equivalent
  • 2 years clinical research coordinator experience 
  • Rheumatology Experience Preferred
  • Must be able to sit for long periods of time
  • Demonstrated experience applying quality controls to electronic clinical research systems to ensure accurate, complete, and timely data
  • Expensive working knowledge of relevant electronic systems, including eSource, CTMS, eReg, and Microsoft 365 
  • Strong understanding of good clinical practice, FDA regulations, & data integrity principles (e.g., ALCOA/C+) with an ability to translate them into system configuration, workflows, and user guidance
  • Proficiency building and interpreting operational quality metrics and dashboards

Apply