Multisite Clinical Research Associate & Site Monitor

IQVIA; Camden (NJ); Presencial; USD 95.000 - 177.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring across multiple sites in the United States. You will ensure protocol adherence, data integrity, and regulatory compliance under GCP/ICH guidelines.

The role requires at least 2 years of on-site CRA experience, strong communication skills, and proficiency with EDC/CTMS systems. Travel may be required and you will collaborate with study teams to drive site performance.

Formación

• Bachelor's degree in a scientific discipline or health care preferred.
• Minimum 2 years on-site CRA monitoring experience.
• Strong knowledge of GCP/ICH guidelines.
• Experience with EDC, CTMS and eTMF systems.
• Excellent written and spoken English.

Responsabilidades

• Perform on-site monitoring visits per protocol and GCP.
• Ensure data quality and regulatory compliance across sites.
• Coordinate training and communications with site staff.
• Track regulatory submissions, approvals, and CRF completion.
• Maintain site documents and TMF/ISF as required.
• Collaborate with study team for project execution and issue resolution.
• Assist in site recruitment strategies and budget considerations.

Conocimientos

CRA with 2+ years on-site monitoring

GCP & ICH knowledge

English proficiency

Organizational skills

Problem-solving

Teamwork & collaboration

Communication skills

Educación

Bachelor's Degree in scientific discipline or health care

Herramientas

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

EDC

CTMS

eTMF

IVRS/IWRS

Descripción del empleo

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring across multiple sites in the United States. You will ensure protocol adherence, data integrity, and regulatory compliance under GCP/ICH guidelines.

The role requires at least 2 years of on-site CRA experience, strong communication skills, and proficiency with EDC/CTMS systems. Travel may be required and you will collaborate with study teams to drive site performance.