Clinical Research Site Manager, On-Site

This is a fully on-site leadership position within the Site Network Group, Avacare located at our site in Pleasant View, Utah.

Lead Clinical Trial Operations at Our Utah Sites!

Join our dynamic team in Pleasant View, Utah, as a Site Manager. Drive clinical trial success with your leadership, strategic thinking, and team-building skills. Be a key player in advancing medical research and achieving corporate goals.

Job Overview

This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, "can-do" attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. The employee, working closely with study team members, will achieve study objectives and corporate goals.

Essential Functions

• Oversee site operations and staff training
• Collaborate with Business Development on study placement
• Ensure enrollment success and develop recruitment strategies
• Coordinate multiple therapeutic area studies
• Conduct 1:1 meetings and annual reviews with staff
• Perform quality control checks and work with Quality Assurance
• Schedule and manage patient/research participant activities
• Collect and maintain source documentation
• Perform data entry and query resolution
• Support collection and review of essential study documents
• Ensure compliance with protocols and regulatory guidelines
• Obtain informed consent and ensure participant safety
• Facilitate site qualification, initiation, monitoring, and close-out activities
• Ensure proper handling of laboratory specimens
• Attend leadership and management training

Qualifications

• Must have clinical skills experience with patients to obtain vitals and perform procedures such as blood draws, EKG, etc.
• Must demonstrate the ability to fulfill responsibilities of CRC II
• Extensive knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
• Superior knowledge and experience of site operations and the drug development process
• Trained in leadership, project management and process development
• Experience training and onboarding new team members including Research Assistants and Clinical Research Coordinators

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 $75,000.00 - $125,000.00. 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.