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Lumen Clinical

Clinical research and site management

Study coordination from protocol preparation through site close-out.

Discuss your study

From site feasibility to study coordination

Clinical research preparation brings together protocol requirements, site capabilities and the study timeline. Feasibility and site selection, submission documents, study start-up and clinical monitoring are connected activities. Lumen Clinical coordinates this work with sponsors and research sites, with responsibilities defined for the study.

  • Protocol development and site feasibility
  • Ethics committee and regulatory submissions
  • Study start-up and clinical monitoring
  • Data management

What to share for an initial discussion

These details help us consider site readiness, submissions and daily site activities within the same schedule. Topics that are still undecided can be discussed during the first meeting.

  • Study objectives, draft protocol and current stage
  • Planned sites, number of centres and target start date
  • Support needed for feasibility, submissions, site coordination, data management and monitoring