Sr. Clinical Trial Manager
C. R. Bard - New Hope, MN

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This position will participate in multi-disciplinary project teams to plan and execute successful clinical studies in support of corporate objectives. The successful Sr. Clinical Trial Manager will demonstrate expertise in all areas of clinical study development and execution, an ability to build and direct effective multi-disciplinary project teams, and an ability to effectively develop personnel by driving competence throughout the clinical affairs organization.

Summary of Position with General Responsibilities:
Oversee the planning and execution of clinical studies to ensure that deliverables are completed on time and within budget
•Select and manage external vendors/CROs to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work
•Ensure that clinical study teams fulfill their responsibilities in accordance with the scope of work and project plan and in compliance with corporate standards, regulations, and Good Clinical Practices
•Interact with investigative sites, vendors and other functional areas to execute the clinical trial
•Coordinate the development and submission of clinical reports and clinical study data
•Identify and demonstrate a comprehensive understanding of competitive landscapes for assigned products and therapeutic areas
•Demonstrate understanding of Lutonix general business functions, products, and procedures and serve on multi-disciplinary project teams as a clinical subject matter expert
Essential Job Functions:

Travel of up to 20-30% required

Basic Qualifications:

4+ years of experience in managing clinical research studies
2+ years of experience managing personnel is preferred
5 + years experience with peripheral vascular devices is preferred
Strong working knowledge of Good Clinical Practices (GCP), FDA regulations, and current industry practices related to the conduct of clinical trials

Additional Desirable Qualifications Skills and Knowledge:
  • Excellent communication skills (oral and written)
  • Strong computer skills
  • Proficiency with MS Windows based applications
  • Strong interpersonal and organizational skills

Education and/or Experience:
  • BA/BS (MA/MS preferred) in health science field or equivalent combination of training and experience
  • 8+ years of experience in the Clinical Research Industry

Physical Demands:

While performing the duties of this job, the employee is regularly required to stand, walk, sit and use hands to manipulate, handle or feel objects, tools, controls and office equipment. The employee frequently is required to talk and hear. The employee is occasionally required to reach with hands and arms and stoop, kneel or crouch.

About this company
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C. R. Bard is no upstart in the world of medical devices. The company has been in the business for more than a century and introduced the...