The role includes coordinating and supporting projects, monitoring project timelines, maintaining c documentation, and ensuring activities are carried out in accordance with applicable regulatory requirements, and company procedures. The candidate will coordinate with vendors, and other stakeholders to track project progress, manage documentation, follow up on deliverables, and support the timely completion of clinical research activities. Qualification:
• Coordinate clinical research projects and monitor timelines, milestones, and deliverables.
• Support clinical trial activities, study documentation, and project-related reporting.
• Ensure compliance with applicable regulatory requirements, SOPs, and ICH-GCP guidelines.
• Coordinate with internal teams, external stakeholders, vendors, and project managers.




• Track project progress, identify delays, and communicate updates to management.
• Support preparation of project reports, meeting minutes, and status updates.
• Assist in managing project schedules, resources, and operational requirements.
• Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Healthcare, or a related field.
• Positive documentation, coordination, and organizational skills.
• Proficiency in MS Office, particularly Excel, Word, and PowerPoint.
• Strong communication skills and the ability to coordinate with multiple stakeholders.

📌 Clinical Research Associate (New Delhi)
🏢 Intrinseque Health
📍 New Delhi