C. R. Bard, Inc.

  • Clinical Trial Manager

    Posted Date 2 months ago(9/19/2018 2:56 PM)
    Industry / Category
    Clinical Trail Manager
    Job ID
    Career Level
    Lutonix, New Hope, MN
    US-MN-New Hope
  • Overview

    Trailblazing Innovation for Patients

    BD is a global medical technology company that is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We lead in patient and healthcare worker safety, and technologies that enable medical research and clinical laboratories. Our innovative solutions help advance medical research and genomics, enhance the diagnosis of infectious disease and cancer, improve medication management, promote infection prevention, equip surgical and interventional procedures, optimize respiratory care and support the management of diabetes.

    Our Minneapolis location, Lutonix, is a design center focused on the advancement and continuous success of Lutonix Drug Coated Balloon, one of BD’s prized Peripheral Intervention products.  Our culture is a natural home for driven, strategic and proactive people who want to follow our motto of Trailblazing Innovation for Patients.  Lutonix utilizes collaborative, cross functional teams that operate globally; our team is committed to making a difference in patients’ lives around the world. This is a place you can find a career with meaningful purpose – advancing the world of health through your successes.

    Summary of Position with General Responsibilities

    The individual in this position will participate on multi-disciplinary project teams to plan and execute successful clinical studies in support of corporate objectives. The Clinical Trial Manager will demonstrate proficiency in all areas of clinical study development and execution, with an ability to build and direct effective multi-disciplinary project teams.

    Essential Job Functions

    • Oversee the planning and execution of clinical studies to ensure that deliverables are completed on time and within budget
    • Develop and manage study related documents and materials such as investigational plans, case report forms, study manuals, monitoring plan, informed consents, websites, recruitment materials and other study related tools
    • Interact with investigative sites through training and ongoing communication to ensure successful execution the clinical trial
    • Assist with oversight of clinical trial monitoring including attendance at qualification, initiation, monitoring, and close-out visits as needed
    • Oversee the appropriate reporting and documentation of adverse events and protocol deviations per investigational plan requirements
    • Plan investigator and coordinator meetings and prepare and present meeting materials
    • Ensure that internal and external clinical study teams fulfill their responsibilities in accordance with corporate standards, regulations, and Good Clinical Practices
    • Select and manage external vendors/CROs to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work
    • Participate on cross-functional core project team to ensure clinical deliverables are aligned with corporate objectives
    • Develop an understanding of competitive landscapes for assigned products and therapeutic areas
    • Demonstrate understanding of Lutonix general business functions, products, and procedures
    • Coordinate the development and submission of clinical reports and abstracts/manuscripts
    • Oversee development and management of clinical database
    • Provide work direction to study team and may manage Clinical personnel

    Basic Qualifications

    • BA/BS
    •  6+ years of experience in the Clinical Research Industry
    • Strong computer skills with a proficiency with MS Windows based applications
    • Strong working knowledge of Good Clinical Practices (GCP), FDA regulations, and current industry practices related to the conduct of clinical trials
    • Excellent communication skills (oral and written)
    • Strong interpersonal and organizational skills and the ability to manage multiple tasks
    • Ability to work independently and provide work direction to others
    • Able to travel 20% on average and up to 40% during peak periods

    Additional Desirable Qualifications Skills and Knowledge

    • 2 + years experience with peripheral vascular devices
    • 2+ years experience in managing clinical research studies
    • Previous experience with EDC systems
    • Device/drug combo technology experience
    • Experience managing direct reports preferred
    • Demonstrated ability to work effectively on cross-functional team
    • 2+ years of experience managing personnel is preferred 

    Physical Demands

    While performing the duties of this job, the employee may be required to stand, walk, sit and use hands to manipulate tools, controls and office equipment. Work may involve continuous computer use with repetitive motion to wrists, hands and fingers.  The employee frequently is required to see, talk and hear.  The employee is occasionally required to bend, lift, reach or stoop.  Inability to meet one or more of these physical demands will not automatically disqualify a candidate or employee from the position.  Upon request, the company may make reasonable accommodations. 

    Work Environment

    While performing the duties of this job, the employee may be in an open cubicle environment. Employee must be able to work in a team-oriented, fast-paced environment.  Bard Lutonix is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.


    This job description is intended as a summary of the primary responsibilities of and qualifications for this position. The job description is not intended as inclusive of all duties an individual in this position might be asked to perform or of all qualifications that may be required either now or in the future.



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