Clinical Research Associate, CRA

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Pfizer

10,000+ employees

Founded 1849

💰 Post-IPO Debt on 2023-05

We’re celebrating 175 years of daring scientific innovation—and we’re not done yet. Every day, we’re channeling our passion and resources into delivering innovative therapies that change the face of healthcare. Let’s outdo yesterday.

📋 Description

• Coordinate and support clinical trial activities, assisting managers in their execution. • Contribute to project tasks and milestones, organizing work to meet deadlines. • Work in a structured environment using established procedures, seeking guidance from colleagues. • Maintain the Pfizer Trial Master File (PTMF) in compliance with ICH-GCP and SOPs, and ensure team members update tracking and files as needed. • Timely update trial and site information in the Corporate Clinical Trial Registry and support Clinical Trial Applications to ethics committees and regulatory authorities. • Provide administrative support for protocols and Informed Consent Documents (ICD) to global Project Managers and Study Managers, assisting with activities within set timelines. • Develop and maintain local tracking spreadsheets for study-related documents, data, and activities, prepare supportive materials for sites, attend training programs, and identify process improvements for inspection readiness and PTMF compliance.

🎯 Requirements

• BA/BS with any years of experience • Demonstrated ability to introduce new ideas and knowledge on all relevant Standard Operating Procedures • Ability to prioritize multiple tasks and develop strategies for the completion of all required activities • Strong organizational skills and attention to detail • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)

🏖️ Benefits

• Health insurance • Flexible work arrangements • Professional development opportunities

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