In-House Clinical Research Associate

Job Summary

To support clinical trials, the full-time In-House Clinical Research Associate will manage data within the clinical trials management system (CTMS), assist with regulatory document collection, and collaborate with project teams, all while working remotely.

Key responsibilities

• Collect, track, and review investigational site records and regulatory documents
• Assist in the development of study plans and status reports
• Perform data reviews and support CRAs with query resolution to ensure compliance with protocols and regulations

Required qualifications

• Bachelor's Degree in a life science, nursing, or pharmacy field with at least 1 year of relevant experience
• Good knowledge of the clinical research process and ICH GCP guidelines
• Desire to grow into a traveling CRA role
• Strong communication skills for effective collaboration and presentation
• Commitment to quality and attention to detail in scientific standards