Sponsor‑Dedicated Clinical Research Associate

IQVIA; Newark (DE); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking an on-site monitoring professional in the United States to ensure sites conduct studies per protocol, regulatory guidelines, and sponsor requirements. You will perform monitoring visits, drive recruitment plans, manage data queries, and maintain essential documentation.

Collaboration with study teams is required to support project execution and quality outcomes. Preferred qualifications include a BS in a scientific field and at least 2 years of on-site monitoring experience,

Qualifications

• Bachelor's Degree in a scientific discipline or health care preferred.
• Requires at least 2 years of on-site monitoring experience.
• Good knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Proficiency with Microsoft Word, Excel and PowerPoint; laptop and mobile devices used.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and GCP.
• Track recruitment and data management to meet project needs and enhance predictability.
• Administer protocol training to sites and maintain regular communication.
• Ensure site documents and TMF/ISF are maintained per regulatory requirements.
• Collaborate with study team members to support project execution.

Skills

GCP knowledge

English fluency

Time management

Problem solving

Education

Bachelor's degree

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking an on-site monitoring professional in the United States to ensure sites conduct studies per protocol, regulatory guidelines, and sponsor requirements. You will perform monitoring visits, drive recruitment plans, manage data queries, and maintain essential documentation.

Collaboration with study teams is required to support project execution and quality outcomes. Preferred qualifications include a BS in a scientific field and at least 2 years of on-site monitoring experience,