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 AD/MGR Project Management

Details
Country: USA
Location: Ridgefield CT
Total applied: 40
Location:US-CT-Ridgefield

Base Pay:N/A
Employee Type:Full-Time Employee

Industry:Healthcare - Health Services Pharmaceutical Biotechnology

Manages Others:no
AD/MGR Project Management

Job Department: Project ManagementJob Category: Biotechnology and PharmaceuticalJob Description:
Boehringer Ingelheim is a family-owned company that is in the business of providing our customers with pharmaceutical and animal health products that significantly enhance their health and improve their quality of life. Our most important resource is our committed, creative and determined employees whose energy is focused on discovery, development and delivery of our innovative products to those who need them. The employees of Boehringer Ingelheim are our most important competitive advantage. Our global presence and thinking provides the opportunity for employees to work internationally and on teams, offering them visibility and the ability to influence the direction and outcome of critical projects. Competitive benefit and compensation programs reflect the Company’s high regard for its employees and enhance each person’s ability to balance the demands of work and personal responsibilities. Every employee at Boehringer Ingelheim contributes to the company’s uncompromising commitment to quality in our products, excellence in our scientific pursuits and high ethical standards of behavior. The diversity of our employees makes it possible for us to craft unique solutions to today’s complex business challenges. We are an equal opportunity employer. M/F/D/V.Duties and Responsibilities:
Monitor, report and analyze timelines to ensure trial, project and major deliverables for assigned area within America’s Region are completed within agreed timelines and cost, and with the expected quality.
Interact with upper management, (as necessary)
Identify issues and facilitate resolution of conflicts between functional groups while maintaining objectivity
Effectively liaise interdepartmentally
Complete multiple tasks/projects simultaneously, while working under pressure
Monitor and challenge resource and budgetary needs for optimal integration of timing, scope and resources
Monitor process inconsistencies and help to build in efficiencies
REQUIREMENTS
Requirements:Bachelor’s Degree in quantitative field with 8-10 years experience or Masters Degree with 5-7 years experience in Pharmaceutical Industry for AD level
Excellent analytical skills and critical thinking abilities
Project management experience desirable
Very good computer skills and ability to learn new systems, excellent understanding of Clinical Trial Management Systems highly desireable
Proven leadership skills and strategic problem-solving ability
Excellent organizational skills and ability to accomplish multiple tasks of varied complexity simultaneously
Proactive ability to predict issues and problem solving abilities
Excellent knowledge of drug development process
Strong communication, interpersonal, and negotiation skills

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