Clinical Research Associate

About the Role

Pfizer is hiring a Clinical Research Associate to monitor Phase II–IV clinical trials across multiple therapeutic areas. You will ensure study sites comply with protocols, GCP guidelines, and regulatory requirements.

Key Responsibilities

• Conduct site initiation, interim monitoring, and close-out visits
• Verify source data and ensure accuracy of case report forms
• Identify and resolve protocol deviations in collaboration with investigators
• Maintain detailed monitoring reports and escalate issues appropriately
• Train site staff on study procedures and data entry standards

Requirements

• Bachelor's in Life Sciences, Nursing, or a related field
• 2+ years of CRA monitoring experience in a pharma or CRO setting
• Strong knowledge of ICH/GCP guidelines and FDA regulations
• Willingness to travel up to 50% of the time

What We Offer

• $32–$46/hr with annual performance bonuses
• Flexible hybrid work arrangement with travel support
• Medical, dental, and vision insurance from day one
• Pfizer stock plan and 401(k) employer match