Sponsor-Focused CRA: Site Monitoring & Management

IQVIA Inc; Sonora; On-site; MXN 1,390,000 - 3,684,000; Full time

Job summary

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. We seek an experienced Clinical Research Associate to monitor sites, ensure study data quality, and support regulatory submissions in alignment with the study protocol and sponsor requirements.

Qualifications include a minimum of 2 years on-site CRA experience, GCP/ICH knowledge, and proficiency with EDC/CTMS/eTMF/IVRS/IWRS systems.

Qualifications

• Minimum 2 years on-site CRA experience in CRO, sponsor, or similar setting.
• Bachelor's degree in science/healthcare preferred.
• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Proficient in Word, Excel and PowerPoint; comfortable with laptop/mobile devices.
• Experience using EDC, CTMS, eTMF, IVRS/IWRS and related trial systems.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, close-out) per scope and GCP.
• Collaborate with sites to drive and track subject recruitment plans.
• Administer protocol training and maintain regular communication with sites.

Skills

CRA experience

GCP/ICH knowledge

Regulatory understanding

Communication skills

Data management

Education

Bachelor's degree in science or healthcare

Experience/education equivalent

Tools

EDC

CTMS

eTMF

IVRS/IWRS

Job description

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. We seek an experienced Clinical Research Associate to monitor sites, ensure study data quality, and support regulatory submissions in alignment with the study protocol and sponsor requirements.

Qualifications include a minimum of 2 years on-site CRA experience, GCP/ICH knowledge, and proficiency with EDC/CTMS/eTMF/IVRS/IWRS systems.