Clinical Research Associate

Job Summary

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