Associate Director, Regulatory Affairs
New
I
IQVIAClinical Research
United StatesFull-TimeManager
SalaryUSD 103600 - 288600 / year
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Job Details
- Experience
- At least 6 years regulatory experience including 3 years management experience
- Required Skills
- Project ManagementBusiness DevelopmentPeople ManagementMicrosoft Office
Requirements
- Bachelor's or Master's Degree in Lifescience or a related discipline.
- At least 6 years of regulatory experience.
- At least 3 years of management experience.
- Specific regulatory or technical expertise.
- Demonstrated success in leading teams or supervisory capacity.
- Solid interpersonal communication skills (oral and written).
- Strong organizational skills and ability to manage competing priorities.
- Proficiency with Microsoft Office applications.
- Advanced negotiating and influencing skills with a flexible, adaptable approach.
- Ability to work on several projects simultaneously while retaining quality and meeting timelines.
- Practical knowledge in leading and managing the execution of processes, projects, and tactics.
Responsibilities
- Manage staff in accordance with organization’s policies, planning and directing work, appraising performance, and guiding professional development.
- Handle personnel issues, conflict management, and define staff goals and expectations independently.
- Coordinate projects and resources to ensure quality deliverables to customers.
- Contribute to business strategy implementation and set site-specific objectives.
- Manage financial responsibility and accountability for one or more Regulatory Affairs sites.
- Lead moderate to significant improvements in processes, systems, or products to enhance job area performance.
- Act as a Project Manager for large, stand-alone programs and manage meetings with regulatory agencies.
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