Job Description

Pfizer seeks a Clinical Research Associate to manage and monitor assigned investigator sites across clinical trials. The role ensures patient safety, regulatory compliance, and quality study execution through site oversight, investigator relationships, and cross-functional coordination from initiation through database lock.

Responsibilities

• Manage site operations from initiation through database lock, ensuring timelines and quality deliverables
• Conduct remote and onsite monitoring activities, including site initiation, routine monitoring, and closure
• Serve as primary contact for assigned investigator sites and facilitate communication across study team
• Resolve protocol-related issues, data queries, and adverse event reporting within required timeframes
• Provide site staff training, coaching, and protocol guidance to ensure compliance and patient safety

Requirements

• Bachelor's degree in life sciences, nursing, pharmacy, or medical background
• Minimum 1 year of clinical research site monitoring and management experience
• Knowledge of ICH/GCP guidelines, FDA, and local country regulations
• Fluency in English and native language(s) of assigned country
• Understanding of clinical trial methodologies and regulatory requirements
• Preferred experience in oncology, vaccines, internal medicine, or infectious diseases
• Global clinical trial experience preferred

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