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Sr Scientist, Bio Clinical Development
Responsible for overall study design, execution, and reporting to earn label claims and new product licenses/marketing authorizations for vaccines consistent with the project goals and in compliance with CVB and USDA and Corporate standards for data integrity and animal welfare.
Work constructively within project teams to represent clinical team's expertise to assure animal studies are designed and executed appropriately to assess clinically meaningful parameters of host animal efficacy and safety, that personnel skillfully administer test article, accurately collect and record relevant data on well-designed case report forms suitable for prompt data entry & analysis that provides a solid foundation for valid study conclusions.
Skillfully collaborate across functions to assure biological clinical activities for project teams deliver efficient, error free study planning and execution while achieving continuous improvement in quality, speed and value of processes supporting clinical trials including protocol and CR Forms, test article availability & suitability, monitoring effectiveness, statistical analysis, study event tracking, and compliance.
Support, coach and train colleagues, especially research associates/monitors, on best practices for study execution with flawless speed and compliance, professional & collaborative team member behaviors, accountability, and alignment within Bio Clinical and with all stakeholders.
A Doctoral degree in Veterinary or related field is required.
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