Clinical Research Associate

A company is looking for an In-House Clinical Research Associate. Key Responsibilities Collect, track, and review investigational site records and regulatory documents Maintain the clinical trials management system (CTMS) and assist with data reviews Coordinate with CRAs and perform monitoring activities, both on-site and remotely Required Qualifications Bachelor's Degree in a life science, nursing, or pharmacy field At least 1 year of experience managing essential documents in the CRO, pharma, or biotech industry Good knowledge of the clinical research process and ICH GCP guidelines Desire to grow into a traveling CRA role Commitment to quality and a collaborative team spirit