The role involves managing communication between sponsors, investigational sites, and internal stakeholders, preparing and maintaining study documentation, and contributing to risk assessment and mitigation plans. The individual will also support the development and execution of project timelines, assist with regulatory and ethics submissions, and participate in continuous improvement of clinical operations processes. Qualifications
• Candidates should possess solid knowledge of clinical trial Protocols and their practical implementation.
• Candidates should possess hands-on experience as Clinical Research Associates and familiarity with site monitoring activities.
• Candidates should possess a solid understanding of Clinical Trials, including phases, regulatory requirements, and GCP guidelines.




• Candidates should possess skills in Research and data documentation to support high-quality, compliant trial conduct.
• Candidates should possess experience in Clinical Operations, including site management, vendor coordination, and supply chain support.
• Relevant academic background in life sciences, pharmacy, medicine, or a related field.
• Strong organizational, time management, and project coordination abilities.
• Effective written and verbal communication skills, with the ability to work collaboratively across multidisciplinary teams.

📌 CRA/Project Management (India)
🏢 Intrinseque Health
📍 India