Project Management
Strong project management is an essential part of running a successful trial. Prologue’s project managers have an average of 12 years of clinical research experience and have worked on trials involving most types of solid tumors and hematologic malignancies. We believe this gives us one of the most experienced PM teams in the industry. Given our exceedingly high retention rate of 90%, you can be highly confident that the assigned PM will see your project through from start to finish.
As the primary point person, the PM is responsible for overseeing all client/CRO interactions, managing study sites, coordinating investigator payments, monitoring study metrics, training, assuring adherence to timelines, and coordinating interactions among Prologue’s operations teams. Prologue has a unique site management model in that the PM is responsible for site management of the study. This model ensures that a knowledgeable person is always available for answering site queries regarding eligibility questions or evaluation issues, and also assures consistency of response across sites.
Accurate, timely, and proactive communication is key to a study’s success.
To this end, PMs initiate and/or oversee:
- Regular team teleconferences
- Project oversight meetings
- Provision of GCP compliance input
- Telephone contact with sites
- Production of newsletters
- Tracking and updating of regulatory documentation
- Distribution and tracking of IND safety reports
Our PMs produce regular written project management status reports. In addition, clients have 24/7 access to real-time study data through our web portal, “ProLink,” which allows them to view investigator site reports, enrollment reports, safety status reports, and data metrics reports.
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