Field Monitoring Specialist for Clinical Trials

IQVIA; Abilene (TX); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring across assigned study sites in the United States. You will ensure protocol adherence, regulatory compliance, and data integrity while communicating with site staff and study teams.

Leverage your CRA experience to manage site visits, trainings, and documentation, including the TMF/ISF, while maintaining strong relationships with sponsors and sites. This role emphasizes quality, timelines, and collaboration.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Minimum 2 years of independent on-site monitoring experience as a CRA in CRO, sponsor, or similar setting.
• Equivalent combination of education, training and experience may be accepted.
• Good knowledge of GCP and ICH guidelines and regulatory requirements.
• Good therapeutic and protocol knowledge as provided in company training.
• Proficiency in MS Word, Excel and PowerPoint; comfortable with laptops and mobile devices.
• Experience using EDC, CTMS, eTMF, IVRS/IWRS and other clinical trial systems.
• Strong written and verbal English communication; able to document clearly.
• Strong organizational and problem-solving skills; able to manage multiple sites.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and GCP.
• Collaborate with sites to drive subject recruitment plans to improve predictability.
• Administer protocol training and maintain regular lines of communication with sites.
• Evaluate site practices for protocol adherence and regulatory compliance; escalate issues.
• Track regulatory submissions, recruitment, CRF completion and data queries; support start-up as needed.
• Maintain TMF and ISF documentation per regulatory requirements.
• Create and maintain documentation of site management activities and visit findings.
• Coordinate with study team members for project execution support.
• Support development of recruitment plans and site-level financial management where applicable.

Skills

Communication skills

English proficiency

Organizational skills

Time management

Problem solving

Education

Bachelor's Degree in scientific discipline or health care

Tools

EDC systems

CTMS

eTMF

IVRS/IWRS

Microsoft Word

Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring across assigned study sites in the United States. You will ensure protocol adherence, regulatory compliance, and data integrity while communicating with site staff and study teams.

Leverage your CRA experience to manage site visits, trainings, and documentation, including the TMF/ISF, while maintaining strong relationships with sponsors and sites. This role emphasizes quality, timelines, and collaboration.