In-House Clinical Research Associate
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
ā¢ Support day-to-day clinical trial operations through remote site management and communication
ā¢ Serve as a primary point of contact for study sites, ensuring timely issue resolution and data quality
ā¢ Review, analyze, and track clinical data for accuracy, completeness, and compliance
ā¢ Assist in oversight of CROs and/or field CRAs to ensure study progress and performance standards
ā¢ Maintain study documentation, trackers, and reports in clinical systems
ā¢ Collaborate cross-functionally to support study timelines and deliverables
ā¢ Quickly learn and navigate clinical technologies and systems; troubleshoot basic technical issues
ā¢ Communicate effectively, synthesizing large amounts of information and sharing key updates
Qualifications
ā¢ Experience as a Clinical Trial Assistant (CTA) and/or In-House CRA required
ā¢ Prior experience as a Clinical Research Coordinator (CRC) is a plus
ā¢ Strong ability to review and interpret large volumes of clinical data efficiently
ā¢ Excellent communication and organizational skills in a fast-paced, multitasking environment
ā¢ Tech-savvy with the ability to quickly learn new systems and tools
ā¢ Proactive, adaptable, and eager to take on a broad range of responsibilities
ā¢ Must work Eastern Time Zone (EST) hours**
Apply Now
Apply Now
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
ā¢ Support day-to-day clinical trial operations through remote site management and communication
ā¢ Serve as a primary point of contact for study sites, ensuring timely issue resolution and data quality
ā¢ Review, analyze, and track clinical data for accuracy, completeness, and compliance
ā¢ Assist in oversight of CROs and/or field CRAs to ensure study progress and performance standards
ā¢ Maintain study documentation, trackers, and reports in clinical systems
ā¢ Collaborate cross-functionally to support study timelines and deliverables
ā¢ Quickly learn and navigate clinical technologies and systems; troubleshoot basic technical issues
ā¢ Communicate effectively, synthesizing large amounts of information and sharing key updates
Qualifications
ā¢ Experience as a Clinical Trial Assistant (CTA) and/or In-House CRA required
ā¢ Prior experience as a Clinical Research Coordinator (CRC) is a plus
ā¢ Strong ability to review and interpret large volumes of clinical data efficiently
ā¢ Excellent communication and organizational skills in a fast-paced, multitasking environment
ā¢ Tech-savvy with the ability to quickly learn new systems and tools
ā¢ Proactive, adaptable, and eager to take on a broad range of responsibilities
ā¢ Must work Eastern Time Zone (EST) hours**
Apply Now
Apply Now