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Job Description & How to Apply Below
You will manage the day-to-day activities of Toxicology and Safety Pharmacology study contracts, coordinating shipments and reviewing invoices to maintain smooth operations. Your solid organizational skills will be key, as you archive study data and keep operations compliant with regulatory guidelines. Be part of a company dedicated to innovative therapies in neurological and endocrine health.
Key Responsibilities:
• Conduct daily Toxicology study management
• Facilitate Test Article shipments in collaboration with teams
• Approve CRO invoices and manage related documentation
• Review tracking database for completeness and accuracy
• Coordinate archival data storage with CROs
Requirements:
• Bachelor's degree; background in biotechnology or pharma
• Proven experience with Toxicology/CRO studies
• Excellent communication and organizational skills
• Ability to resolve operational challenges
• Strong time management skills
Combine your expertise and passion at Neurocrine to enhance our transformative work.
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