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Experienced Clinical Research Associates for your trials

Scientific rigor and regulatory compliance are essential in clinical trials. Keena Life Sciences provides seasoned Clinical Research Associates who support your projects at every stage of monitoring, on-site or remotely.

The role of our Clinical Research Associates in the field

Our CRAs work directly with investigator sites. Their mission covers several operational areas:

check_circleAccurate verification of data and its traceability

check_circleMonitoring compliance with Good Clinical Practice and internal procedures

check_circleOngoing collaboration with investigator teams to anticipate operational difficulties

check_circleChecking eligibility criteria and monitoring participant recruitment

check_circleRapid detection of deviations and implementation of appropriate corrective actions

Expertise available whenever you need it

Our Clinical Research Associates integrate into your organization as one-off reinforcement or for the full duration of the study. This outsourcing model adapts to activity peaks, unplanned absences, or ongoing needs on a multicentric trial.

Every assignment is managed with a constant focus on preserving the scientific integrity of your data. Our CRAs help secure the conduct of your trials while supporting the performance of your internal teams.

Our implementation method

Every assignment begins with a scoping conversation: scope of sites, protocol, sponsor-specific requirements and tools already in place. This step allows us to select the CRA profile best suited to your therapeutic area.

Once the assignment is underway, we organize regular progress meetings with your team covering visit status, identified deviations and ongoing corrective actions. The frequency of these meetings adjusts to the criticality of the current phase.

For one-off or ongoing CRA reinforcement, contact us to assess your needs.

When should you outsource your Clinical Research Associates?

Outsourcing becomes relevant as soon as a site lacks the availability to ensure close follow-up. It's also relevant during a multicentric activity peak or when specific therapeutic expertise is required.

Our Clinical Research Associates then join your team without any continuity gap, across France as well as on international studies.

Using external Clinical Research Associates also helps smooth out a monitoring workload that varies significantly across study phases, without adding weight to your permanent structure.

This flexibility avoids rushed internal hiring, often hard to justify for a few months' assignment. It lets you keep a lean core team while guaranteeing continuous site follow-up.

Need CRA reinforcement to secure your timeline?

Our team supports sponsors and CROs in this exact situation.

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