Sponsor-Dedicated Clinical Research Associate

IQVIA; Iowa (LA); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking a field-based monitor to manage site activities and ensure adherence to the study protocol and regulatory requirements. You will perform site visits, train site staff, and uphold data quality across multiple sites.

Responsibilities include tracking regulatory submissions, patient recruitment, CRF completion, and responding to data queries. Strong communication and organizational skills are essential for collaboration with study teams and vendors.

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 and ICH guidelines.
• Proficiency in Microsoft Word, Excel and PowerPoint.
• Written and verbal communication in English.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and GCP.
• Collaborate with sites to drive and track subject recruitment per project needs.
• Administer protocol training and establish regular communication with sites.
• Evaluate site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion, data queries, and start-up support as needed.
• Maintain TMF/ISF documentation and site files per regulatory requirements.
• Coordinate with study team for project execution support.

Skills

On-site monitoring experience

English proficiency

Organizational skills

Problem-solving

Time management

Financial management

Team collaboration

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking a field-based monitor to manage site activities and ensure adherence to the study protocol and regulatory requirements. You will perform site visits, train site staff, and uphold data quality across multiple sites.

Responsibilities include tracking regulatory submissions, patient recruitment, CRF completion, and responding to data queries. Strong communication and organizational skills are essential for collaboration with study teams and vendors.