In-House Clinical Research Associate

The In-House Clinical Research Associate will develop study documents and tools, support sites in obtaining IRB approval, respond to regulatory board requests, ensure all required site regulatory documents are in place, conduct routine file reviews, analyze site performance problems, provide ongoing training for study sites, maintain regular communication with study sites, conduct remote review of data on electronic Case Report Forms (eCRFs), work closely with field CRAs and data management to resolve queries, assist with efforts to recruit investigative sites, and comply with ICH GCP guidelines, FDA regulations, and company SOPs. They will also participate in meetings and manage conflicting priorities to deliver on commitments.