
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.
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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.
• 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.
• 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)
• Health insurance • Flexible work arrangements • Professional development opportunities
Apply Now🕒 July 3
Clinical Research Associate II at ICON, conducting clinical trial monitoring and ensuring data integrity in a fast-paced environment. Collaborating with site staff and contributing to study documentation.
🕒 July 2
Clinical Research Associate I monitoring clinical trials for ICON. Delivering high-quality outcomes through coordination and compliance in clinical trial operations.
🕒 July 2
CRA II at ICON designing and analyzing clinical trials. Engaging in site qualification and monitoring, ensuring compliance with clinical trial processes.
🕒 June 24
CRA I at ICON delivering clinical trial monitoring work and coordinating clinical trial operations in Buenos Aires. Ensuring compliance with procedures, protocols, and regulatory requirements while building relationships with stakeholders.
🕒 June 18
Clinical Research Associate II responsible for monitoring and analyzing clinical trials for ICON. Collaborating with investigators and ensuring data integrity and safety measures throughout the trial process.