On-site study coordination

We provide solutions for clinical sites with resource needs. Depending on the assignment, responsibilities and tasks can include:

  • Support in organisation, coordination and performance of clinical trials and research-associated activities.
  • Maintaining and updating study/regulatory binders
  • Completion of Case Report Forms
  • Coordination in process, storage and transport of study medication and samples
  • And much more!

Interested? Get in touch!