Job Description
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**