Job Overview

We are seeking a dedicated and experienced Site Manager to join our team!

Please note, this is full-time, on-site position in Las Vegas, NV.

Qualifications

• Bachelor’s degree in a related field and/or 4 or more years of equivalent experience (Site Management / Site Manager)
• Must have experience as a Clinical Research Coordinator
• Prior leadership/management experience required.
• Clinical skills: Phlebotomy, Vitals (BP, ECG)
• Knowledge of medical terminology
• Experience in patient contact.

Key Responsibilities

• Oversees the conduct of their assigned site; responsible for the training of staff/providers, process development, point of contact for the Directors of Operations and cross-functional teams.
• Works closely with Business Development and Feasibility on study placement
• Accountable for enrollment success at sites across all studies; works to understand revenue expectations.
• Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved.
• Maintains significant depth of knowledge and experience in coordinating across multiple therapeutic areas.
• Ability to coordinate as primary CRC on at least six studies of medium to high complexity, as well as back-up CRC on other studies when needed.
• Conducts 1:1 meetings and annual reviews with site staff.
• Assists in the development of the annual site roadmap.
• Completes all protocol related training.
• Performs quality control checks on source documentation and regulatory.
• Works closely with Quality Assurance Department to ensure quality at site; creates processes and CAPAs to improve trends.
• Performs patient/research participant scheduling.
• Collects patient/research participant history.
• Collects and maintains source documentation.
• Performs data entry and query resolution.
• Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.).
• Adheres to an IRB approved protocol.
• Obtains informed consent of research subjects.
• Supports the safety of research subjects, reports adverse events.
• Coordinates protocol related research procedures, study visits, and follow-up
• Facilitates site qualification, study initiation, and monitoring visits, and study close-out activities.
• Ensures proper collection, processing, and shipping of laboratory specimens.
• Attends training(s) on leadership, communication, and other topics to help in the management of teams, as required.

Join us and contribute to our mission of delivering excellent service and achieving outstanding results!

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.