Manager Clinical Monitoring, Spain - Madrid Indiferente

  • Confidencial
  • Madrid
  • 09-10-2016
  • Otros
Location: Office-based in Madrid, Spain Position: Permanent contract, full-time Major responsibilities: - Manage professional employees who work on clinical trial projects. - Ensure compliance to policies, SOPs, federal and local guidelines and GCPs. - Identify, address and follow up on performance and quality issues. - Track and report both departmental and customer metrics Provide business development support. - Provide input into financial forecasts and review invoices for accuracy. - Complete Quality Assessment Visits QAV for assigned CRA/monitoring staff - Participate in the interview process. - Review and approve expense reports and timesheets. - Coordinate and conduct new employee orientation and training. Supervisory/Management responsibilities: - Supervise, coach and mentor staff - Oversee development of direct reports by setting goals, conducting performance reviews, evaluating and monitoring training needs, creating development plans, mentoring, and coaching - Set priorities and schedule activities of departmental resources, implement company objectives, and create alternative solutions to address business and operational challenges Requirements: - Bachelors degree in a related field or equivalent combination of education, training and experience - Five to seven years of experience in clinical research and preferably in the same functional department - Demonstrates strong leadership and line management potential - Extensive knowledge of GCP/ICH guidelines and other applicable regulatory requirement - Strong time management, technical and organizational skills - Knowledge of basic financial concepts as related to forecasting and budgeting - Must demonstrate good computer skills - Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade - Ability to travel as necessary up to 50%

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