Senior Clinical Research Associate

Role Overview

Reporting to the ANZ GSSO Leadership, you will play a critical role in delivering high-quality clinical trials by partnering with investigator sites to ensure patient safety, regulatory compliance, and operational excellence.

What You Will Do

Lead site management and monitoring activities, conduct onsite, remote, and risk-based monitoring activities, and support patient recruitment and enrollment efforts.

Why It Might Be a Fit

You will help accelerate the delivery of clinical research while maintaining the highest standards of quality and Good Clinical Practice. You will also contribute to successful enrollment, data integrity, database release, and the generation of evidence that advances innovative medicines for patients worldwide.

Requirements

• Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
• Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
• Valid driver’s license and passport required

Benefits

• Paid parental leave
• Access to Health & Wellness apps
• Career Growth Experiences program
• Recognition & rewards program
• Paid volunteer days
• Life Insurance Benefits
• Pfizer Learning Academy access to top content providers
• Access to flu vaccines & skin checks
• Options to purchase additional leave
• Salary packaging & novated lease options

Originally posted on Himalayas