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₹1,300,000 Per Year
₹2,000,000 Per Year
Analyzes drug safety data from clinical trials and post-marketing surveillance. Prepares detailed reports on adverse events and contributes to safety assessments. Requires strong analytical skills and proficiency in safety databases.
₹1,100,000 Per Year
₹1,900,000 Per Year
Leads a team in monitoring drug safety and ensuring compliance with regulatory agencies. Oversees the preparation of safety reports and implements risk management strategies. Requires leadership skills and extensive pharmacovigilance experience.
₹1,500,000 Per Year
₹1,600,000 Per Year
Handles the collection, processing, and reporting of adverse drug reactions (ADRs). Works closely with clinical teams to ensure timely and accurate data submission. Requires strong attention to detail and knowledge of regulatory standards.
₹800,000 Per Year
₹2,200,000 Per Year
Responsible for monitoring and analyzing drug safety data, including adverse events. Ensures compliance with regulatory requirements and performs risk assessments. Requires experience in data analysis and knowledge of pharmacovigilance regulations.
₹700,000 Per Year
₹1,800,000 Per Year
Job Description
The Clinical Data Assoc...
₹800,000 Per Year
₹1,000,000 Per Year
Responsible for collecting, reviewing, and process...
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