Age limit 20 to 30 Clinical Study Design Execution Leading the design and implementation of clinical study protocols and monitoring their progress Regulatory Compliance Ensuring all activities from clinical trials to post-market evaluations adhere to regulatory requirements and guidelines e g FDA regulations GCP Data Management Analysis Overseeing the collection interpretation and reporting of clinical data to ensure its accuracy and integrity Cross-Functional Collaboration Working with various departments including R D regulatory affairs quality risk management and marketing to integrate clinical strategy with product development Investigator Site Management Recruiting and managing relationships with clinical trial investigators and research sites Regulatory Submissions Preparing the clinical sections of documents for regulatory submissions and providing clinical information for other reports Product Lifecycle Support Providing scientific evidence and insights throughout the product s lifecycle including during post-market surveillance Job Types Full-time Permanent Fresher Pay 38 160 05 - 52 536 72 per month Perks Food provided Work Location In person

📌 Clinical Affairs (Tamil Nadu)
🏢 Meshira luxury
📍 Tamil Nadu