Clinical Project Management for your local and international studies
Keena Life Sciences offers full Clinical Project Management, from planning to operational coordination. Our project managers work on local studies as well as international multicentric trials.
Structured Clinical Project Management at every phase
We work across the full lifecycle of your study, with coordination tailored to each phase:
Well-managed multicentric coordination
Our project managers centralize communication between sponsor, investigator sites and providers. They ensure compliance with contractual deadlines and quality standards defined upstream of the study.
This coordination limits delays caused by communication breakdowns between the various stakeholders in a multicentric trial.
Risk management built into project coordination
Our project managers identify potential concerns specific to your protocol upstream: low-recruiting sites, dependence on a critical provider, or country-specific regulatory requirements.
This anticipation allows the project management plan to be adjusted before these risks affect your overall timeline. Every identified deviation is documented and tracked until resolved.
To structure the coordination of your study, our clinical project management experts are available for a conversation arrow_forwardWhen should you outsource your Clinical Project Management?
Outsourcing is relevant when your internal team lacks the availability to coordinate a multicentric trial. It's also relevant when facing a demanding regulatory area, such as rare diseases or medical devices.
Clinical Project Management entrusted to Keena Life Sciences adapts to your existing organization. Whether you need a project manager for reinforcement or full-scale coordination, our team aligns with your internal processes.
We also step in to support an internal project manager already in place, focused on a specific phase such as site activation or an audit. This model avoids duplicating responsibilities already handled internally.