International Clinical Project Manager

Are you working in Clinical Trials and want to be in a new role? Do you have experience as Project Manager coordinating international clinical trials? If you have said yes to both questions, in Valesta we have your new role.


  • Establishment of collaborative relationships with Cooperative groups/CROs with respect to the study management
  • Act as Operational point contact.
  • Work in close collaboration with Cooperative groups/CRO to ensure projects are executed in a timely manner and to high quality, proactively identifying issues and  solutions to ensure projects remain on track
  • Ensure contracts execution in timely manner
  • Act as primary contact for Drug Supply process including provision of forecasting
  • Liaise closely with other functions such as Regulatory, Drug Safety
  • Track progress of study & provide monthly updates on status to all internal stakeholders
  • Ensure adequate and timely filing of documentation.
  • Coordinate, Support and Follow up the concept approval process as needed (local and international)
  • Development, implementation and maintenance of Working Procedures to promote high quality, efficient, and compliant systems for study management
  • On an as required basis, organize meetings with Affiliates/Partners and all relevant people in order to provide, training, discussion forums and sharing of best practice
  • Provide support and guidance to Regional Medical Liaison and Medical Affairs personnel as required

Requirements of the position:

  • Experience in project management
  • Excellent command of medical and scientific areas assigned
  • Experience in study/site set up
  • Leadership and negotiation skills
  • Experience in coordinating international clinical trials
  • Experience in oncology therapeutic area would be desirable
  • LifeScience university degree

What we offer?

  • Perm contract in an investigation/medical center
  • Good salary range and benefits

Application form : International Clinical Project Manager

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