Associate Director of Bioanalytical Principal Investigation

Other jobs >> General

Negotiable

Permanent

Description

Recruiter Covance



Location Green Bay, Wisconsin (US)



Salary Competitive



Posted 17 Oct 2019



Closes 14 Nov 2019



Ref COVAGLOBAL34978EXTERNAL



Discipline Clinical, Bioinformatics, Analysis & Statistics, Quality, Operations, Administration



Result Type Jobs



Position Type Permanent



Hours Full Time



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Job Overview:Who we are and what we do:Covance is a global, world-leading Life Science Contract Research Organization that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical *********** Covance, we offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. We put our trust in science and in one another. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner, as Covance has helped pharmaceutical and biotech companies develop one-third of all prescriptions medicines in the market today. The Role:Our Madison, Wisconsin site is currently recruiting for anAssociate Directorof Principal Investigation . As the Associate Director your will ensure the delivery of the Small Molecule Bioanalytical scientific strategy, collaborating with Head of Sciences, Operational leadership, and SMEs. You will also have responsibility for:Oversight of staff located in Madison, Wisconsin.Consults with clients on studies placed with the Small Molecule Regulated Bioanalytical Department.Executes a strategic plan, in consultation with the Director, which identifies the areas in which the department will concentrate its Study Management efforts and capital where applicable to meet business growth objectives. Tactically assigns resources within the Study Management group (personnel, space, equipment), implements programs, and drives process improvement to assure financial and budget expectations are met.Bioanalytical Regulatory expert to ensure GxP compliance standards are maintained as appropriate.Drives the departments customer service endeavors and effectively manages their team to ensure successful resolution of client needs in a timely manner.Serves as bioanalytical management representive both within the organization and externally as appropriate.Initiates, plans and implements staff development programs within the Study Management group. Develops capabilities and resources to meet both present and future needs within this group.Implements appropriate affirmative action, salary administration, and communication programs within the group. Creates an employee empowered work environment that is stimulating and rewarding, yet deals with poor performance in a decisive fashion.Performs other related duties as assigned.Education/Qualifications:Ph.D. in Chemistry or related fieldExperience in industry or CRO may substitute for educationExperience:Eight years related experience in addition to PhD degree. Drug development experienceGLP knowledge and experienceSkilled in performing presentations.Skilled time management, planning and budgeting.Experienced in leading and developing people.



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