Project Management
Marken’s intensive project management approach means that your project moves seamlessly through the clinical trial process.
We provide services beginning with the receipt of your clinical trial supplies, continuing on to Pick, Pack & Distribution, and then to collection, reconciliation, storage, and destruction of returns. At Marken, we practice a structured approach to project management:
Initiation
The project is assigned to a dedicated project manager responsible for ensuring full understanding of study specific requirements.
Planning
Prior to the study’s start, our team defines and documents the scope of services required among all participating depots and regional project managers.
Execution
Initial receipt of material; QC, verification and release; pick & pack and initial shipments to sites
Control
Value-added tools are utilized to ensure control; status reports, sponsor meetings, program meetings, KPIs and on-line inventory status.
Closing
The Solo™ system guarantees that all investigational medical products and data accounted for allowing for ease in study closure and drug destruction.
Every Marken customer has a single point of contact during the lifespan of their project: the Global Project Director. The Global Project Director provides global oversight of trials run and is tasked with the overall satisfaction of Marken’s performance across all trials. Additionally, each project has a Regional Project Leader, who manages day-to-day study activities and progress reporting.
To find out more about how Marken’s project management solutions can help your clinical trial process, email info@marken.com or fill out our short contact form:
