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Clinical Trial Projects Manager Dublin Ireland,  

DS Biopharma (company)

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.  

  • 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  


Leopardstown Dublin Ireland

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