Sponsor-Driven Clinical Research Associate

Iqvia; Melbourne; Sur place; AUD 108 000 - 287 000; Plein temps

Résumé du poste

IQVIA is seeking an on-site Clinical Research Associate to monitor trial sites in Australia, ensure protocol adherence, and manage data submission. You will coordinate recruitment, maintain TMFs, and liaise with the study team to support start-up activities.

The role requires at least 2 years' CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS tools. Excellent communication and time management are essential.

Qualifications

• Bachelor's degree preferred in science or health care.
• At least 2 years' on-site CRA monitoring experience.
• GCP/ICH and regulatory requirements knowledge.
• Proficient with MS Word, Excel and PowerPoint; good English.

Responsabilités

• Perform site monitoring visits per scope of work and GCP.
• Coordinate recruitment and tracking to meet project needs.
• Manage TMF/ISF documentation and site files.
• Collaborate with study team and support start-up activities.

Connaissances

GCP/ICH knowledge

On-site CRA experience

Regulatory know-how

English communication

Time/financial management

Formation

Bachelor's degree in scientific discipline or health care

Outils

EDC systems

CTMS

eTMF

IVRS/IWRS

Word

Excel

PowerPoint

Description du poste

IQVIA is seeking an on-site Clinical Research Associate to monitor trial sites in Australia, ensure protocol adherence, and manage data submission. You will coordinate recruitment, maintain TMFs, and liaise with the study team to support start-up activities.

The role requires at least 2 years' CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS tools. Excellent communication and time management are essential.