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
Benefits:
Food provided
Work Location: In person
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