Clinical Trial Site Monitor & Data Integrity Lead

IQVIA; Bellingham (WA); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking a Site Monitoring professional to ensure that study sites conduct and report data per protocol, regulations, and sponsor requirements. You will perform monitoring visits and coordinate with sites to support recruitment and data quality.

Responsibilities include managing site documents, tracking regulatory submissions, and maintaining TMF/ISF in compliance. Strong English communication and GCP/ICH knowledge are required.

Qualifications

• Requires at least 2 years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Proficiency with site regulatory documents and TMF/ISF.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out).
• Coordinate subject recruitment plans with sites.
• Administer protocol training to sites and maintain communication.
• Track regulatory submissions, enrollment, CRF completion, and data queries.
• Ensure TMF/ISF documents are properly filed and maintained.

Skills

On-site monitoring

GCP/ICH knowledge

Regulatory submissions

English communication

Time management

Financial management

Education

Bachelor's degree in scientific discipline or health care preferred

Tools

Microsoft Word

Excel

PowerPoint

Job description

IQVIA is seeking a Site Monitoring professional to ensure that study sites conduct and report data per protocol, regulations, and sponsor requirements. You will perform monitoring visits and coordinate with sites to support recruitment and data quality.

Responsibilities include managing site documents, tracking regulatory submissions, and maintaining TMF/ISF in compliance. Strong English communication and GCP/ICH knowledge are required.