Clinical project management

A clinical investigation requires dedicated management of resources, documents, and overall study progress. The amount of time necessary for adequate study management, and the influence it can have on costs, timelines, and data quality is often underestimated. Medical device clinical trial management requires project oversight, experience in medical device clinical investigations, operational management, effective communication with sites and monitors.  A hands-on approach.


Qserve's experts are experienced in managing clinical investigations with medical devices from start till end. We know where to expect the pitfalls and how to keep all stakeholders on track. Our team has extensive experience in clinical affairs, study management, and project management, developing and maintaining monitor and site relations.

Adequate and tailored clinical study management will result in a positive return on investment

Clinical study management includes:

  • Developing and maintaining site relationships
  • Resource management
  • Problem solving
  • Progress and deadline compliance

What can we do for you?

Full project management service (protocol to final study report)

Management of contracted monitors or CRO


Interim clinical study management 


Oversight during all study phases

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