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Research Operations Director Jobs in Arizona (NOW HIRING)

Trialsphere Corp

Clinical Research Coordinator

Chandler, AZ · On-site

$60K - $70K/yr

... and operational needs to the Site Director and PI. Escalate medical, eligibility, safety, PI ... The Senior Clinical Research Coordinator is expected to use discretion and independent judgment in ...

Actalent

Clinical Research Coordinator

Phoenix, AZ

$58K - $68K/yr

Coordinate day-to-day clinical trial operations in accordance with study protocols and regulatory ... Direct. Benefits. Workplace Type This is a fully onsite position in Phoenix,AZ. Application ...

IRONWOOD PHYSICIANS,P.C.

Research RN

Chandler, AZ · On-site

Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research. * Screens, consents, enrolls and follows study subjects and oversees the same by non-RN ...

IRONWOOD PHYSICIANS,P.C.

Research RN

Surprise, AZ · On-site

Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research. * Screens, consents, enrolls and follows study subjects and oversees the same by non-RN ...

CommonSpirit Health

Research Scientist I

Phoenix, AZ · On-site

Brad Racette and co-directed by Dr. Chia-Ling Phuah, that aims to harness the power of big data to ... Responsible for operational oversight and implementation of funded Geographic and epidemiologic ...

Bannerhealth

Research Intern

Phoenix, AZ · On-site

General Operations Find your path in health care. We want to change the lives of those in our care ... the direct supervision of a department manager or designee. The position is responsible for ...

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Research Operations Director information

What are the main challenges a research operations director faces in supporting cross-functional research teams?

A Research Operations Director often navigates challenges such as coordinating resources across multiple research projects, ensuring consistent processes, and managing communication between diverse stakeholders like researchers, product managers, and leadership. Balancing the needs of various teams while maintaining research quality and compliance can be complex, especially as organizations scale. Effective directors establish standardized procedures, foster a culture of collaboration, and implement tools that streamline workflows to address these challenges.

What are the key skills and qualifications needed to thrive as a research operations director?

To thrive as a Research Operations Director, you need expertise in research management, process optimization, and budgeting, often supported by an advanced degree in a related field. Familiarity with project management software, compliance systems, and data analysis tools is typically required. Strong leadership, communication, and problem-solving abilities are crucial for leading teams and coordinating complex projects. These skills ensure efficient research operations, compliance with regulations, and the successful delivery of research outcomes.

What is a research operations director?

A Research Operations Director is a senior professional responsible for overseeing the infrastructure, processes, and resources that support research activities within an organization. They manage teams, budgets, and systems to ensure research projects run efficiently and comply with regulatory standards. Their role often includes improving workflow, implementing best practices, and supporting researchers with tools and training. The goal is to streamline research operations and enhance the impact of research outcomes.

What is the difference between Research Operations Director vs Research Manager?

AspectResearch Operations DirectorResearch Manager
CredentialsTypically requires advanced degrees (e.g., Master’s or PhD) and extensive experience in research managementUsually holds a bachelor’s or master’s degree with several years of research experience
Work EnvironmentOversees multiple research teams, manages operations, and aligns research strategies with organizational goalsManages specific research projects or teams, focusing on execution and deliverables
Employer & Industry UsageCommon in large corporations, tech companies, and research institutionsFound across various industries including tech, healthcare, and market research firms

The Research Operations Director focuses on strategic oversight and operational management of research functions, while the Research Manager handles day-to-day project execution. Both roles require research expertise, but the director role involves broader leadership and organizational responsibilities.

What does a research operations director do?

A research operations director oversees the planning, management, and execution of research activities within an organization. They coordinate research teams, ensure compliance with protocols, manage budgets, and optimize processes using tools like research management software to support effective data collection and analysis.
What are the most commonly searched types of Research Operations jobs in Arizona? The most popular types of Research Operations jobs in Arizona are:
What are popular job titles related to Research Operations Director jobs in Arizona? For Research Operations Director jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Research Operations Director jobs in Arizona look for? The top searched job categories for Research Operations Director jobs in Arizona are:
What cities in Arizona are hiring for Research Operations Director jobs? Cities in Arizona with the most Research Operations Director job openings:
Research Operations Director jobs near you
Infographic showing various Research Operations Director job openings in Arizona as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Clinical Research Coordinator

Trialsphere Corp

Chandler, AZ • On-site

$60K - $70K/yr

Full-time

Re-posted yesterday

Job description

Job Title: Senior Clinical Research Coordinator

Position Type: Full-time
FLSA Classification: Exempt, salaried
Location: Chandler, Arizona
Position Summary
TrialSphere Corp. is seeking an experienced Senior Clinical Research Coordinator to independently manage assigned clinical trials from start-up through close-out. This position is responsible for study-level coordination, operational decision-making, sponsor/CRO communication, protocol implementation, subject visit oversight, regulatory readiness, and cross-functional workflow management.
 The Senior Clinical Research Coordinator is expected to exercise independent judgment in managing study priorities, identifying operational and compliance risks, resolving study-related issues, and ensuring assigned trials are conducted in accordance with protocol requirements, ICH-GCP, FDA regulations, sponsor expectations, and site SOPs.
 This is a senior-level position requiring strong clinical research experience, independent problem-solving, and the ability to manage multiple complex trials with minimal day-to-day supervision.
 Essential Duties and Responsibilities

The Senior Clinical Research Coordinator will:
Manage assigned clinical trials from start-up through close-out, including study activation, visit planning, subject flow, sponsor communication, monitoring support, and study close-out activities.
Independently prioritize daily, weekly, and study-level workflows based on protocol requirements, subject safety, enrollment goals, data deadlines, sponsor expectations, and site operational needs.
Serve as a primary operational contact for sponsors, CROs, monitors, vendors, laboratories, imaging partners, and internal site staff for assigned studies.
Review protocols, manuals, visit schedules, and sponsor guidance to determine operational requirements and implement appropriate site workflows.
Identify protocol, operational, recruitment, compliance, and data-quality risks and recommend corrective or preventive actions to management and/or the PI.
Evaluate subject visit requirements and coordinate resources needed for successful visit execution, including investigator availability, assessments, labs, imaging, investigational product, and participant stipends.
Oversee accurate and timely completion of source documentation, EDC entry, query resolution, regulatory documentation, and sponsor-required tracking.
Prepare for and support monitoring visits, audits, sponsor reviews, and inspections by ensuring assigned studies remain inspection-ready.
Train, mentor, and support junior CRCs, research assistants, students, or other team members involved in assigned trials.
Communicate study updates, enrollment barriers, protocol concerns, and operational needs to the Site Director and PI.
Escalate medical, eligibility, safety, PI judgment, or major business decisions appropriately while independently resolving routine and study-operational issues within the scope of the role.
Maintain compliance with ICH-GCP, FDA regulations, HIPAA, IRB requirements, sponsor requirements, and TrialSphere SOPs.
 Decision-Making and Independent Judgment
This position requires the ability to independently evaluate study priorities, determine appropriate operational workflows, resolve study-management issues, assess compliance risks, communicate with external study partners, and make recommendations affecting study performance and quality.
The Senior Clinical Research Coordinator is expected to use discretion and independent judgment in matters of significance related to study conduct, data quality, subject visit operations, regulatory readiness, and sponsor deliverables.
 Qualifications
Minimum 3–5 years of clinical research coordinator experience required.
Prior experience independently managing multiple interventional clinical trials required.
CNS, neurology, Alzheimer’s disease, migraine, movement disorder, or complex Phase II–IV trial experience preferred.
 Strong working knowledge of ICH-GCP, FDA regulations, informed consent, source documentation, EDC systems, monitoring visits, and IRB requirements.
Experience communicating directly with sponsors, CROs, monitors, vendors, and investigators.
Ability to work independently, prioritize competing deadlines, and identify operational or compliance risks.
CCRC, ACRP-CP, CCRP, or similar certification preferred but not required.
 Physical and Operational Requirements
Ability to work onsite in a clinical research environment.
Ability to interact professionally with research participants, caregivers, investigators, sponsors, monitors, and vendors.
Ability to use CTMS, EDC, eReg/eSource, eConsent, email, Microsoft Office, and sponsor portals.
Occasional schedule flexibility may be required based on subject visits, monitoring visits, sponsor deadlines, or study needs.
Equal Employment Opportunity Statement
TrialSphere Corp. is an Equal Opportunity Employer. Employment decisions are based on qualifications, experience, job performance, and business needs, without regard to any protected status under applicable law.