Responsibilities include importing and de-duplicating text files of electronic database search results, managing EndNote library citations, searching for journal articles, retrieving electronic copies, formatting bibliographies and report contents, and performing other related tasks as needed. This position is a great opportunity to learn more about health care research and systematic reviews and is remote.

The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials, supporting the completion and coordination of logistical and administrative tasks. Responsibilities include data collection for regulatory submissions, document tracking, managing the delivery of study supplies, and maintaining relationships with site staff.

This is a remote role responsible for processing medical record requests by taking calls from patients, insurance companies and attorneys to provide medical record status and documenting information in multiple platforms using two computer monitors in a high-volume production environment. Proficient in Microsoft office (including Word and Excel) is needed.

The In-House CRA coordinates aspects of clinical monitoring and site management in accordance with ICH Good Clinical Practices, FDA/MHRA/EMA guidelines, local regulations and WEP Clinical Standard Operating Procedures, providing operational support to ensure the effective and efficient delivery of clinical site monitoring and regulatory requirements as well as manages required documentation.