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Project Manager - Medical Devices

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About the role

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Project Manager - Medical Devices *LI-MB1

Location: Any EU Location

 

Role summary

Are you a strong Project Manager with experience in Medical Devices? If so, you will be responsible for managing client studies within Clinical Operations and or Clinical Outcomes.

 

Job functions/responsibilities

  • As a Manager, your will recognize the importance of and craft a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs, as well as lead projects in a timely manner in adherence with ICON’s SOP’s, ICH, GCP and appropriate regulation and liaise with other department managers as necessary.
  • Delivery of projects in accordance with the contract, timelines and study budget
  • Identification and review of change orders for the budget
  • Attend and present at client Investigator, Kick-Off and client meetings
  • Enable the study team to improve performance and knowledge. Provide coaching / mentoring as necessary.
  • Development/ Review/ Maintenance of all trial documentation
  • Primary client and CRO contact; develops successful working relationships with client
  • Preparation and management of meeting agendas and minutes
  • Prepare / Approve Project Reports
  • Management of Study Centers
  • Conducts reader training with support of Project Director
  • Ensures all management/ tracking systems are up to date
  • Provide regular feedback to senior management on project status, client satisfaction and staffing issues.
  • Participate in BD activities as appropriate
  • Supports internal, client, and regulatory audits
  • Participate in interview as required
  • Travel (approximately 5%) domestic and/or international
  • Other duties as assigned
  • Supervision
  • Oversight of study
  • Manages Data Management Lead for scheduling and preparation of data deliveries as required
  • Management of eCRF development process

Experience, skills, knowledge requirements 

  • EU/APAC: Prior meaningful experience in clinical trials
  • Deep understanding of Project Management processes
  • Highly developed problem solving skills
  • Good commercial awareness and customer focus
  • Trained in Good Clinical Practices
  • Able to work as team leader and individually on multiple client projects
  • Strong people management and effective interpersonal skills
  • Ability to multi-task
  • Business Computer skills
  • Due to the nature of this position, it may be required for the employee to travel. Therefore, dependent on the employee’s location, the employee may be required to possess a valid driver’s license. 

Education requirements

  • Bachelors Degree or local equivalent in medicine or science beneficial
  • Fluent in written and spoken English. Additional language skills desirable

Next Steps:


Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

 

ICON Plc is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment


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