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Clinical Trial Projects Manager - Ireland  

Company managed [?] Still accepting applications

Posted on : 08 April 2017

Project Description


Main Duties / Responsibilities: 
  • The successful candidate will be required to manage multiple clinical projects to GCP standards.
  •  They will provide oversight of all the responsibilities transferred by company to CROs and other vendors.  
  • They will be responsible for delivering all tasks and projects in a timely manner within budget taking a proactive approach at all times. 
  • They would also be expected to manage and monitor/audit both CROs and related vendors onsite. 
  • Carry out various other additional tasks that may be required from time to time in accordance with the overall goals of the company.  



Requirements: 
  • Relevant Scientific degree with at least 4-5 years’ working in Clinical Research in a Phase I, II CRO and/or pharmaceutical company as a CRA and then CPM. 
  • GCP experience in the pharmaceutical industry 
  • Monitoring and project management experience 
  •  A willingness to deal with international teams working in different time zones 
  • Therapeutic experience and scientific knowledge in Dermatology is a distinct advantage. 
  • A flair for scientific writing (protocols and reports) and fully conversant with the use of EDC in clinical trials 
  • Excellent interpersonal, communication and problem solving skills 
  • Flexible in reacting to changing priorities in projects without compromising timelines and/or quality 
  • Ability to travel (domestic and international) as required