Job Summary
We are seeking a detail-oriented and highly motivated In-House Clinical Research Associate to support clinical trial operations in a dynamic biotechnology environment. This role is ideal for someone eager to grow, take on diverse responsibilities, and thrive in a fast-paced team that wears many hats. The IHCRA will focus on remote site management, data review, and study coordination while ensuring high-quality execution and compliance.
Responsibilities
• Support day-to-day clinical trial operations through remote site management and communication
• Serve as a primary point of contact for study sites, ensuring timely issue resolution and data quality
• Review, analyze, and track clinical data for accuracy, completeness, and compliance
• Assist in oversight of CROs and/or field CRAs to ensure study progress and performance standards
• Maintain study documentation, trackers, and reports in clinical systems
• Collaborate cross-functionally to support study timelines and deliverables
• Quickly learn and navigate clinical technologies and systems; troubleshoot basic technical issues
• Communicate effectively, synthesizing large amounts of information and sharing key updates
Qualifications
• Experience as a Clinical Trial Assistant (CTA) and/or In-House CRA required
• Prior experience as a Clinical Research Coordinator (CRC) is a plus
• Strong ability to review and interpret large volumes of clinical data efficiently
• Excellent communication and organizational skills in a fast-paced, multitasking environment
• Tech-savvy with the ability to quickly learn new systems and tools
• Proactive, adaptable, and eager to take on a broad range of responsibilities
• Must work Eastern Time Zone (EST) hours**