Clinical Research Associate

Responsibilities

• Coordinate and support all activities related to clinical trials, assisting managers in their execution
• Assist in site activation activities, including gathering necessary documentation
• Review data for quality and completeness to ensure timely submission to data management
• Support patient safety and eligibility monitoring
• Coordinate with sites to finalize budget worksheets and contractual agreements
• Maintain accurate site-level information on the clinical trials registry
• Support the study team with regulatory submissions and maintain the Electronic Library and Records Archive
• Attend investigator meetings as required

Requirements

• BA/BS with at least 2 years of experience or MBA/MS with any years of experience
• Knowledge of International Conference on Harmonization Good Clinical Practices (ICH-GCP) and local regulations
• Deep understanding of quality and regulatory requirements across various countries
• Proficiency in applications used in clinical trials
• Expertise in SOP compliance and relevant standard operating procedures
• Effective verbal and written communication skills with fluency in English
• Demonstrated success working within matrix organizations

Preferred Qualifications

• Master's degree combined with relevant therapeutic area experience
• High level of project management, analytical, and problem-solving skills
• Strong organizational, time management, and attention to detail skills
• Proficiency in Microsoft SharePoint and SharePoint Designer
• Experience using generative AI tools to support problem solving and enhance productivity

About the Company

Pfizer is a global leader in healthcare, dedicated to empowering decisions regarding the safe and appropriate use of medicines. We strive to improve patient care and treatment efficacy by ensuring our scientific evidence is robust and providing essential medical insights to transform millions of lives.