HMR Technologies

Clinical Research

• Correspond with research sponsors, CROs, and other research organizations regarding study initiation and ongoing study activities
• Prepare, complete, and submit required study documentation and regulatory materials
• Assist in preparing reports for analysis and submission to study sponsors
• Organize and manage clinical trial agreements, budgets, and confidentiality disclosures
• Respond to study-related correspondence, including protocol inquiries and information requests
• Support the successful conduct of assigned clinical studies in accordance with regulatory requirements, guidelines, and internal policies
• Assist with identification, resolution, and follow-up of site-related issues
• Assist in the preparation of study materials and provide training support for electronic systems or devices
• Contribute to the review, maintenance, and development of standard operating procedures (SOPs)
• Provide additional administrative or research support as requested by clinical management

Clinical Research Coordinator