Lead Clinical Trial Operations at Our Scottsdale Site!

This is a fully on site leadership position within the Avacare site network group. Join Avacare’s dynamic and mission-driven team in Scottsdale, AZ, as a Site Manager. In this leadership role, you’ll drive clinical trial success through strategic oversight, operational excellence, and team development. Be a key contributor to advancing medical research and achieving organizational goals.

Overview

As Site Manager, you will oversee the daily operations of our clinical research site, ensuring studies are conducted in compliance with regulatory guidelines and internal standards. You’ll lead a high-performing team, collaborate cross-functionally, and play a pivotal role in study execution across multiple therapeutic areas.

Essential Functions

Lead and manage site operations, including staff training and development

Partner with Business Development to evaluate and place new studies

Develop and implement patient recruitment strategies to ensure enrollment success

Oversee multiple concurrent studies across various therapeutic areas

Conduct regular 1:1 meetings and annual performance reviews

Perform quality control checks and collaborate with Quality Assurance

Manage scheduling and coordination of patient/research participant activities

Ensure accurate source documentation, data entry, and query resolution

Support collection and review of essential study documents

Maintain compliance with study protocols, GCP/ICH, and regulatory requirements

Obtain informed consent and ensure participant safety and well-being

Facilitate site qualification, initiation, monitoring, and close-out visits

Ensure proper handling and processing of laboratory specimens

Participate in leadership and management training programs

Qualifications

Hands-on clinical experience including obtaining vitals, performing blood draws, EKGs, etc.

Associate Degree or higher preferred

Proven success as a lead Clinical Research Coordinator (CRC) with experience managing concurrent studies

Demonstrated ability to fulfill responsibilities equivalent to a CRC II or higher

Extensive knowledge of GCP/ICH guidelines and clinical trial regulations

Strong understanding of site operations and the drug development lifecycle

Experience in leadership, project management, and process improvement

Skilled in onboarding and training new team members, including Research Assistants and CRCs 

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $62,400.00 - $156,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.