Salt Lake City, Utah, United States
20 hours ago
Clinical Research Site Manager, On-Site

This is a fully on-site leadership position within the Site Network Group, Avacare.

Lead Clinical Trial Operations at Our Utah Sites!

Join our dynamic team in Bountiful or Salt Lake City, 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

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.https://jobs.iqvia.com/covid-19-vaccine-status

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.
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