Clinical Trials Site Lead

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

Job summary

IQVIA is seeking a Clinical Research Coordinator to support conduct of clinical trial activities in accordance with regulatory requirements. The role works closely with study teams to achieve objectives and corporate goals.

Responsibilities include overseeing site conduct, training staff, coordinating enrollment strategies, and ensuring quality across studies. Opportunities exist to travel to CCT locations as needed.

Qualifications

• Experience assisting in clinical trial activities and coordinating with study teams.
• Strong knowledge of GCP/ICH and applicable regulations.
• Ability to train site staff and coordinate with Directors of Operations and cross-functional teams.

Responsibilities

• Oversees the conduct of assigned site and trains staff/providers.
• Works with Business Development and Feasibility on study placement.
• Drives enrollment success and understands revenue targets across studies.
• Develops and implements patient recruitment strategies to meet targets.
• Maintains knowledge across multiple therapeutic areas and studies.
• Coordinates as primary CRC on several studies and backups on others.
• Conducts 1:1 meetings and annual reviews with site staff.
• Supports site qualification, initiation, monitoring, and close-out activities.

Skills

Logical thinking

Prioritization

Can-do attitude

Adaptability

Interpersonal skills

Team building

Clinical skills

Job description

IQVIA is seeking a Clinical Research Coordinator to support conduct of clinical trial activities in accordance with regulatory requirements. The role works closely with study teams to achieve objectives and corporate goals.

Responsibilities include overseeing site conduct, training staff, coordinating enrollment strategies, and ensuring quality across studies. Opportunities exist to travel to CCT locations as needed.