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Job Description & How to Apply Below
Explore a rewarding career as a Senior Clinical Research Associate I at Pfizer, managing clinical trials and ensuring patient safety and compliance across multiple sites. Your expertise is crucial for quality outcomes.
In this central role, you will oversee the execution of clinical trials, ensuring compliance with regulatory standards and Pfizer's operational goals. By managing relationships with investigators, you will support the effective recruitment of study participants and monitor trial progress, enhancing both patient safety and satisfaction. Your contributions will also include training site staff on compliance with protocols.
Key Responsibilities:
• Oversee clinical sites from initiation to closeout
• Ensure compliance with all regulatory requirements
• Facilitate investigator communication and training
• Manage site-related issues for swift resolution
• Prepare comprehensive reports on study progress
Requirements:
• Bachelor’s in a life sciences field
• Minimum 3 years of monitoring experience required
• Experience in therapeutic areas preferred
• Proficiency in both English and local languages
• Willing to travel extensively (60-80%)
Advance your career at Pfizer, ensuring the highest standards in clinical research and patient care.
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Position Requirements
10+ Years
work experience
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