Join Pfizer as an Oncology Clinical Research Associate I, focusing on trial site management and monitoring. This full time position emphasizes quality execution and patient safety in clinical studies.

In this Senior Clinical Research Associate I role, you will actively manage the operational aspects of clinical trials at designated research sites. Your responsibilities will include monitoring compliance with protocols, addressing trial-related issues, and ensuring that patient safety remains a top priority. You’ll also work closely with investigators, fostering effective communication to promote successful trial outcomes.

Key Responsibilities:
• Oversee clinical trial operations from initiation to closeout
• Interact with site staff to ensure protocol compliance




• Execute onsite and remote monitoring as needed
• Track and report trial progress and site metrics
• Support recruitment efforts and resolve activation challenges

Requirements:
• Degree in life sciences or relevant field
• At least 3 years of monitoring experience in clinical research
• Background in oncology, vaccines, or infectious diseases preferred
• Bilingual in English and local language
• Deep knowledge of GCP and FDA regulations

Make meaningful contributions to Pfizer’s clinical research initiatives and enhance patient care outcomes.
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📌 Oncology Clinical Research Associate I Role Ontario (Canada)
🏢 Pfizer
📍 Canada