📌 Job Title:
Clinical Research Site Manager
Location: Glendale, Arizona
Job ID: R1501182
Job Type: Full-Time
Work Setup: Fully On-site (Office-based)
Job available in additional locations
🔗 Apply Now | Save Job | Share via Email | LinkedIn | Facebook
🧭 Overview
Join Avacare, part of the IQVIA site network, as a Site Manager at our Glendale, AZ clinical research facility. This on-site leadership role is ideal for experienced Clinical Research professionals ready to lead operations, optimize performance, and drive results across multiple therapeutic areas.
You will:
Provide day-to-day leadership at the site level
Ensure clinical trial success through quality, compliance, and operational excellence
Lead and mentor a growing team of clinical staff
🔑 Essential Functions
🔹 Leadership & Oversight
Lead and manage daily site operations
Conduct regular 1:1s and annual performance reviews
Train, mentor, and onboard new staff (e.g., CRCs, Research Assistants)
Support leadership and management training initiatives
🔹 Study & Site Management
Oversee multiple concurrent studies across various therapeutic areas
Partner with Business Development to evaluate and place new studies
Coordinate patient/research participant activities and scheduling
Ensure compliance with protocols, ICH-GCP, and regulatory requirements
Perform quality control checks and collaborate with Quality Assurance
🔹 Patient Enrollment & Data Integrity
Develop and implement patient recruitment strategies
Ensure accurate and complete source documentation and data entry
Resolve queries in a timely and compliant manner
Obtain informed consent and ensure participant safety
🔹 Sponsor & Regulatory Collaboration
Support collection and review of essential study documents
Facilitate site qualification, initiation, monitoring, and close-out visits
Oversee proper collection, handling, and processing of lab specimens
🎓 Qualifications
Required:
Hands-on clinical experience, including:
Vital signs
Blood draws
ECG/EKGs
Proven success as a Lead Clinical Research Coordinator (CRC)
Experience managing multiple concurrent clinical studies
Advanced understanding of GCP/ICH guidelines and clinical trial regulations
Familiarity with the drug development lifecycle
Demonstrated project management and team leadership skills
Preferred:
Associate Degree or higher in a relevant field
CRC II level or above experience
Background in process improvement and staff training
💼 Compensation & Benefits
Annual Salary Range: $62,400 – $156,000
Actual pay is based on experience, skills, location, and schedule
May include:
Incentive plans and bonuses
Health and welfare benefits
Additional forms of compensation
🌐 About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare analytics. We connect data, technology, and expertise to accelerate the development of innovative treatments that improve lives.
🔗 Learn more: https://jobs.iqvia.com
⚖️ Equal Opportunity Statement
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or other legally protected status.
🔗 EEO Policy
📩 Ready to apply?
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