Clinical Site Operations Lead

IQVIA LLC; Bountiful (UT); On-site; USD 65,000 - 162,000; Full time

Job summary

IQVIA LLC in the United States is seeking a site-based Clinical Research Coordinator/Operations professional to support multicenter clinical trials. You will train site staff, develop processes, and coordinate with Directors of Operations and cross-functional teams to drive enrollment and regulatory compliance.

The role demands GCP/ICH knowledge, leadership, and project management. You will oversee enrollment, patient recruitment strategies, scheduling, source documentation, data entry, and QA

Qualifications

• Must have clinical skills experience with patients to obtain vitals and perform procedures such as blood draws, EKG, etc.
• 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

Responsibilities

• Oversee site conduct and train staff/providers.
• Accountable for enrollment success across studies and revenue understanding.
• Develop and implement patient recruitment strategies to meet targets.
• Coordinate as primary CRC on at least 6 studies of medium to high complexity.
• Conduct 1:1 meetings and annual reviews with site staff.
• Support development of annual site roadmap and protocol training.
• Perform quality control checks on source documentation and regulatory.
• Coordinate scheduling and data entry to support study documents.

Skills

Clinical skills

GCP/ICH knowledge

Leadership

Project management

Process development

Communication

Team building

Site operations

Job description

IQVIA LLC in the United States is seeking a site-based Clinical Research Coordinator/Operations professional to support multicenter clinical trials. You will train site staff, develop processes, and coordinate with Directors of Operations and cross-functional teams to drive enrollment and regulatory compliance.

The role demands GCP/ICH knowledge, leadership, and project management. You will oversee enrollment, patient recruitment strategies, scheduling, source documentation, data entry, and QA