Clinical Trial Site Management Services
Our clinical trial management team coordinates resources, training, and collaboration across all phases of your study. We work as an extension of your team to keep projects efficient and compliant.
Your dedicated project manager serves as the central point of contact. With scientific and therapeutic expertise, they guide your study from start-up through completion, whether conducted in our own clinical trial units or through our network of qualified external sites.
On-Time and On-Budget Clinical Trial Management
Our project managers coordinate every stage of your clinical trial, from Phase 1b through IIb, with a focus on accuracy, efficiency, and clear oversight. We develop timelines, monitor endpoints, and manage budgets to keep studies on track and compliant.
Our project management team will:
- develop project plans and timelines
- coordinate start-up activities to initiate sites efficiently
- oversee study conduct and clinical monitoring
- lead and support tasks from protocol development through clinical study report preparation, whether managed in-house or with vendors
- maintain accurate pharmacometric deliverables
- manage budgets and oversee vendor selection through established clinical trial site evaluation and selection processes
Explore More of Altasciences’ CRO Services
Advancing your drug candidate smoothly to proof of concept is what we do best.