Senior Central Monitor

📋 Description

• Perform remote site monitoring and management activities for assigned projects in accordance with
• Support clinical monitoring teams in implementing study strategies, initiatives, processes, and
• Collect, analyze, and organize study data and generate reports covering areas such as recruitment
• Support data risk assessments and centralized monitoring activities throughout the study lifecycle.
• Maintain communication with clinical sites and relevant internal and external stakeholders as
• Assist with document collection, visit preparation, study data review, and other monitoring

🎯 Requirements

• Bachelor’s degree preferred; candidates without a formal degree may be considered based on
• At least 3 years of experience in study coordination, in-house monitoring, or relevant experience
• Working knowledge of clinical trial execution processes and centralized monitoring practices.
• Familiarity with systems such as Electronic Document Management Systems (EDMS), Electronic Data
• Understanding of general quality assurance concepts and practices.
• Strong organizational skills and exceptional attention to detail.

🎁 Benefits

• Fully remote work opportunity within the United States.
• Collaborative environment supporting innovation, professional development, and cross-functional
• Opportunities to contribute to clinical research and support the development of new therapies.
• Inclusive workplace focused on diversity, equity, belonging, and employee empowerment.
• Opportunities to develop expertise in centralized monitoring, clinical data review, risk-based
• Hybrid flexibility may be available for employees located within a reasonable commute of an office