Clinical Trials Site Monitor & Manager

IQVIA; Melbourne (FL); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking an on-site Clinical Research Monitor to ensure sites conduct studies per protocol, GCP and ICH guidelines. You will manage visits, recruitment plans, training, and communication with sites, while maintaining essential study documentation and TMF/ISF files.

Ideal candidates have 2+ years of on-site monitoring experience, strong English communication, and proficiency with MS Word, Excel, and PowerPoint. This is an in-country role requiring residency in the United States.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Requires at least 2 years of on-site monitoring experience.
• Good knowledge of GCP/ICH guidelines.
• Proficient in MS Word, Excel and PowerPoint; laptop and mobile devices.
• Strong written and verbal English communication.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits).
• Drive subject recruitment planning in line with project needs.
• Administer protocol training and maintain regular communication with sites.
• Evaluate site practices for protocol compliance and regulatory adherence.
• Track regulatory submissions, recruitment, CRF completion, data queries; support start-up as needed.
• Maintain TMF and ISF documentation.
• Collaborate with study team for project execution support.
• May support development of site recruitment plans and site financial management where applicable.

Skills

On-site monitoring

Regulatory knowledge

English communication

Time management

Relationship building

Education

Bachelor's Degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking an on-site Clinical Research Monitor to ensure sites conduct studies per protocol, GCP and ICH guidelines. You will manage visits, recruitment plans, training, and communication with sites, while maintaining essential study documentation and TMF/ISF files.

Ideal candidates have 2+ years of on-site monitoring experience, strong English communication, and proficiency with MS Word, Excel, and PowerPoint. This is an in-country role requiring residency in the United States.