Clinical Study and Project Management

Oversight is a critical factor in the successful completion of any study or project. Parexel FSP has teams of highly trained, experienced Study Managers (SM) and Clinical Project Managers (CPM) who are dedicated to the success of your study or project.

  • Clinical Project Manager (CPM):  responsible for executing a clinical trial or clinical programs from protocol design to the final clinical study report.  The CPM coordinates all efforts for the trial across functional groups and supporting vendors. .  Specific functional groups include biostatistics, clinical monitoring, data management, medical writing, medical and safety, to ensure proper conduct and timely completion of all projects.
  • Study Manager (SM): responsible for all study management aspects of assigned studies of limited complexity (e.g., single country, a small number of countries) or manage a unique part of a larger study (e.g., recruitment and retention). The Study Manager leads and manages the tactical execution of one or more clinical studies from study start-up through database release and inspection readiness to ensure timely delivery of quality data.

With a focus on cultivating relationships with both customers and candidates, we rely on our Parexel FSP Culture Mapping ™ process to find the best match to your clinical development needs and company culture as quickly as possible.  

We are always available for a conversation.


Communication Preference

Communication Preference