Clinical Research Associate: Site Monitoring & Study Management

IQVIA; Paradise Valley (AZ); Sur place; USD 75 000 - 198 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data collection per protocol and regulatory requirements. The role involves on-site visits, site management, and collaboration with sponsor teams to support study conduct across locations.

The position requires a Bachelor’s degree in a scientific or health-care field and at least 2 years of independent on-site monitoring experience, with strong English communication and regulatory knowledge.

Qualifications

• Bachelor's degree in scientific discipline or health care.
• Minimum 2 years on-site CRA monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Proficiency with Word, Excel and PowerPoint.
• Experience with EDC, CTMS, eTMF, IVRS/IWRS.
• Excellent written and verbal English.
• Strong organizational and problem-solving skills.
• Ability to manage time and finances.
• Ability to liaise with study team and sponsors.

Responsabilités

• Perform site monitoring visits per scope and GCP.
• Drive subject recruitment plan to fit project needs.
• Administer protocol training and maintain site communications.
• Evaluate site practices for protocol adherence.
• Track regulatory submissions, recruitment, CRFs, data queries.
• Maintain TMF/ISF documentation.
• Collaborate with study team for project execution.
• Support site initiation/start-up activities.
• Assist site financial management as applicable.

Connaissances

English

Communication

Regulatory knowledge

GCP/ICH knowledge

Time management

Teamwork

Formation

Bachelor's Degree in scientific discipline or health care

Outils

EDC

CTMS

eTMF

IVRS/IWRS

MS Word

MS Excel

PowerPoint

Description du poste

IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data collection per protocol and regulatory requirements. The role involves on-site visits, site management, and collaboration with sponsor teams to support study conduct across locations.

The position requires a Bachelor’s degree in a scientific or health-care field and at least 2 years of independent on-site monitoring experience, with strong English communication and regulatory knowledge.