In-House Clinical Research Associate

Alira Health is looking for an In-House Clinical Research Associate to support clinical sites from approval through close-out while working with field CRAs and Clinical Project Managers to help protect trial data quality without frequent travel. The role involves preparing study materials such as informed consent form templates and site binder contents, helping sites with IRB submissions and site-specific consent forms, handling regulatory board questions, checking that all site approvals and documents are complete before investigational product is shipped, and reviewing files in both the site records and the Trial Master File. It also includes looking at site performance issues, giving ongoing training, keeping regular contact with sites about protocol and GCP compliance, reviewing eCRF data remotely, and working with data management to clear data discrepancies. The advert names experience with study documents, regulatory submissions, site oversight, file review, and remote eCRF data review as part of the work. It does not list a specific degree, certification, or number of years of experience. No language requirement is stated. The position is remote and full time. It is aimed at someone who can coordinate across teams, manage site documentation carefully, and support study conduct in a collaborative setting.