Site Manager, On-Site (Clinical Trials)

Location: Bountiful, Utah, United States; on-site

Salary: $64,600–$161,500 annualized base pay

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Oversee assigned clinical trial sites, including staff training, process development, and coordination with operations directors and cross-functional teams.
• Develop and implement patient recruitment strategies, conduct recruitment activities, and support enrollment targets across studies.
• Coordinate complex studies as a primary Clinical Research Coordinator and provide backup CRC support when needed.
• Manage patient scheduling, informed consent, study visits, follow-up procedures, safety reporting, and collection of patient histories.
• Maintain source documentation, perform data entry and query resolution, and support essential study documents and reports.
• Facilitate site qualification, initiation, monitoring, and close-out activities, including laboratory specimen processing and shipping.

Requirements

• Clinical experience with patients, including obtaining vital signs and performing procedures such as blood draws and EKGs.
• Ability to fulfill the responsibilities of a CRC Level II.
• Extensive knowledge of GCP/ICH and applicable clinical research regulations.
• Strong knowledge of site operations and the drug development process.
• Training in leadership, project management, and process development.
• Ability to work on-site in Bountiful, Utah, United States.

Culture & Benefits

• Work closely with study teams, Business Development, Feasibility, Quality Assurance, sponsors, and site staff.
• Participate in leadership, communication, and management training.
• Support quality improvement through process development and corrective and preventive actions.
• Health and welfare benefits may be offered in addition to base pay.
• Occasional travel to other clinical research locations may be required.