Clinical Research Monitor & Site Lead

Regulatory Jobs; Overland Park (KS); On-site; USD 90,000 - 190,000; Full time

Job summary

IQVIA is seeking a field-based clinical research monitor to ensure sites conduct studies per protocol, GCP, and sponsor requirements. You will visit sites, train staff, manage recruitment plans, and track regulatory submissions and data quality across assigned studies.

The role requires a Bachelor's degree in a scientific field, 1.5 years of on-site monitoring experience, and strong English communication, time and financial management skills.

Qualifications

• Bachelor's Degree in a scientific discipline or healthcare field.
• Minimum 1.5 years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Proficient in Microsoft Word, Excel and PowerPoint; familiarity with laptops/tablets.
• Strong English communication; organizational, problem-solving and time/financial management skills.

Responsibilities

• Perform site monitoring visits (initiation, monitoring, close-out) per contract and GCP.
• Collaborate with sites to recruit participants per project needs.
• Administer protocol training and maintain regular communication with sites.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Track regulatory submissions, approvals, enrollment, CRF completion, and data queries.
• Maintain TMF and ISF documents according to GCP and local requirements.
• Create site management documentation and visit reports.
• Coordinate with study team for project execution.
• Support study start-up and site financial management where applicable.

Skills

On-site monitoring

Good communication

Time management

Team collaboration

Problem solving

Education

Bachelor's degree in scientific discipline or health care

Tools

MS Word

MS Excel

PowerPoint

Job description

IQVIA is seeking a field-based clinical research monitor to ensure sites conduct studies per protocol, GCP, and sponsor requirements. You will visit sites, train staff, manage recruitment plans, and track regulatory submissions and data quality across assigned studies.

The role requires a Bachelor's degree in a scientific field, 1.5 years of on-site monitoring experience, and strong English communication, time and financial management skills.