Clinical Research eSource Architect

Job Summary

Responsible for overseeing eSource creation, the full-time Clinical Research eSource Architect will manage the development and distribution of eSource for clinical studies while providing training and mentorship to staff in a remote work environment.

Key responsibilities

• Create eSource for new studies according to protocol specifications
• Distribute eSource to applicable sites and collaborate with local staff to implement site-specific requirements
• Serve as a subject matter expert for eSource creation and mentor clinical sites

Required qualifications

• BA/BS degree preferred
• 2+ years of clinical research experience (CRC, QA, Source, CRA) required
• 2+ years of knowledge in ICH/GCP guidelines and FDA regulations from hands-on work experience required
• Highly self-motivated and a self-starter
• Demonstrated proficiency in Microsoft Office (Word, Excel, PowerPoint, and Outlook)