Senior Clinical Research Monitor

IQVIA; Carlsbad (CA); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA LLC is seeking an on-site Clinical Research Monitor in Carlsbad, CA, to ensure sites conduct studies per protocol and regulations. You will monitor visits, manage site communication, and oversee data quality and submission timelines.

The role requires a Bachelor’s degree in a scientific field or health care and at least 3 years of on-site monitoring experience, with strong knowledge of GCP/ICH and proficient MS Office skills.

Qualifications

• Bachelor's degree preferred in a scientific discipline or health care.
• At least 3 years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Proficient in MS Word, Excel, and PowerPoint.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Drive and track subject recruitment plans to align with project needs.
• Administer protocol training to sites and maintain regular communication with sites.
• Evaluate site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, approvals, recruitment, CRF completion and data queries; may support start-up.
• Ensure TMF/ISF documentation is complete and auditable.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team for project execution support.
• Support development of site-level recruitment plans and, if applicable, site financial management.

Skills

On-site monitoring

Site management

Regulatory knowledge (GCP/ICH)

English communication

Organizational skills

Time management

Financial management

Communication skills

Education

Bachelor's Degree in scientific discipline or health care

Tools

Microsoft Word

Excel

PowerPoint

Job description

IQVIA LLC is seeking an on-site Clinical Research Monitor in Carlsbad, CA, to ensure sites conduct studies per protocol and regulations. You will monitor visits, manage site communication, and oversee data quality and submission timelines.

The role requires a Bachelor’s degree in a scientific field or health care and at least 3 years of on-site monitoring experience, with strong knowledge of GCP/ICH and proficient MS Office skills.