Clinical Research Associate, CRA

🕒 July 16

🇦🇷 Argentina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 50%

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Pfizer

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1849

💼 Consulting

📣 Marketing

💊 Pharmaceuticals

💰 Post-IPO Debt on 2023-05

Consulting • Marketing • Pharmaceuticals

Pfizer is a pharmaceutical company that has been at the forefront of scientific innovation for 175 years. The company is dedicated to improving health and well-being at every stage of life by providing access to safe, effective, and affordable medicines and healthcare services. Pfizer focuses on delivering innovative therapies, particularly in the field of cancer treatments, as it continues to progress in transforming the healthcare landscape.

📋 Description

• Coordinate and support clinical trial activities, assisting managers in execution • Contribute to project tasks and milestones, organizing work to meet deadlines • Work in a structured environment using established procedures and seek guidance from colleagues • Maintain the Pfizer Trial Master File (PTMF) in compliance with ICH-GCP and SOPs • Ensure team members update tracking and files as needed • Update trial and site information in the Corporate Clinical Trial Registry • 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 • Develop and maintain local tracking spreadsheets for study-related documents, data, and activities • Prepare supportive materials for sites and attend training programs • 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 completing required activities • Strong organizational skills and attention to detail • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) • Excellent written and verbal communication skills • Preferred: Experience managing clinical trial and regulatory documents • Preferred: Understanding of International Conference on Harmonization Good Clinical Practices and local regulations • Preferred: Familiarity with applications used in clinical trials • Preferred: Experience with electronic data capture systems • Preferred: Experience using AI tools, including ChatGPT or Microsoft Copilot, for problem solving and productivity; curiosity about responsible AI practices, risk management, and ethical use

🏖️ Benefits

• Equal opportunity employment commitment • Medical benefits (section indicated, with no specific details provided)