What is important to you is important to us: finding the ideal match! For over 20 years Valesta has partnered with clients, candidates and employees to deliver the very best Project Staffing Solutions.

Our goal is to help you find a valuable job, to guide you through the labyrinth of clinical research and to offer you a stimulating learning environment. It is key that you, being a clinical research professional, can further develop your potential and build an interesting career.

We put interesting jobs in the spotlight and bring them directly to you.  Keep in mind Valesta offers a continuous flow of new vacancies within various regions…  So also keep an eye on our Careers page!

Do you know someone who fits the profile? Do you feel you are ready for the next step in your career? Are you interested in finding out more? Don't hesitate to contact us or visit our Careers section to view more opportunities. All job descriptions are available upon request.

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.

Responsabilities:

  • 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