Site Monitoring & Trial Execution Specialist

IQVIA; Mansfield (OH); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking a site monitor to perform monitoring visits, manage site training, and ensure protocol compliance across trials. The role requires coordinating with sites to drive subject recruitment, track regulatory submissions, and maintain TMF/ISF documents in line with GCP and local regulations.

Ideal candidates will have 2+ years of on-site monitoring experience, a relevant scientific or healthcare degree, and strong English communication skills.

Qualifications

• Bachelor's degree in a scientific discipline or health care preferred.
• 2+ years of on-site monitoring experience.
• Strong knowledge of GCP/ICH guidelines.
• Excellent written and verbal English communication.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) per contract scope and GCP.
• Track recruitment plans to enhance predictability.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Manage study progress: regulatory submissions, recruitment, CRF completion, data queries.

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking a site monitor to perform monitoring visits, manage site training, and ensure protocol compliance across trials. The role requires coordinating with sites to drive subject recruitment, track regulatory submissions, and maintain TMF/ISF documents in line with GCP and local regulations.

Ideal candidates will have 2+ years of on-site monitoring experience, a relevant scientific or healthcare degree, and strong English communication skills.