Your Clinical Operations partner for clinical trials
Keena Life Sciences supports pharmaceutical companies, biotechs, medical device manufacturers and CROs in the day-to-day management of their clinical studies.
A Clinical Operations partner built on hands-on clinical expertise
Keena Life Sciences was founded in 2021, drawing on more than ten years of combined clinical development expertise across a wide range of therapeutic areas: oncology, neurology, nephrology, cardiology, ophthalmology, rare diseases, and medical devices.
We support pharmaceutical companies, biotechs, CROs, and medical device manufacturers through every critical stage of their studies: investigator site selection, regulatory submissions, international project management, site activation, site monitoring and oversight, and site close-out. This tailored approach lets our partners navigate the challenges of clinical development with expertise, flexibility, and rigor.
Our clinical development expertise
Our Clinical Operations and FSP expertise combines four complementary areas, available separately or as a hybrid model, to strengthen your teams or take on some or all of your clinical activities.
Clinical Research Associates
Experienced CRAs made available for on-site and remote monitoring.
Clinical Project Management
From planning to operational management of local and international studies.
Regulatory Submission
Preparation and filing of applications with ethics committees, ANSM and relevant authorities.
Dedicated Support
Individualized monitoring and ongoing support.
A flexible outsourcing model
Beyond these four pillars, we offer CPM, CRA, CTA and TEC outsourcing under flexible models. This format adapts to a one-off reinforcement as well as to lasting support throughout a study's lifecycle.
We also step in as a subcontracting partner for other CROs, when an activity spike or a specific therapeutic expertise calls for it. This peer-to-peer collaboration remains discreet and follows the processes already in place at our partner's organization.
A single point of contact for your study
Each assignment is organized around a designated point of contact, responsible for coordinating exchanges between your team and our consultants in the field. This single point of contact simplifies the follow-up of deliverables, KPIs and any potential deviations.
We adapt the frequency of progress meetings to the sensitivity of your timeline: weekly during a critical phase, monthly for ongoing support.
Qualified clinical profiles, across France
Our consultants operate across the entire country, as well as on internationally conducted studies when the protocol requires it. We select each CRA, CPM or TEC profile according to the therapeutic area and regulatory complexity of the project.
This targeted selection limits the consultant's ramp-up time and speeds up their capacity building on your protocol.
To assess your monitoring or team reinforcement needs, our Keena Life Sciences team is available for a conversation.
Trusted by
Our track record
With more than ten years of combined expertise, Keena Life Sciences has established itself as a trusted partner to leading pharmaceutical companies and medical device manufacturers.
10+ years of combined expertise
Built by our experts in study management, data management, and local monitoring before the firm's founding in 2021.
20+ clinical studies and projects supported
Covering Phase I to Phase IV, notably in oncology, cardiology, nephrology, dermatology, and medical devices.
50+ investigator sites
Monitored and coordinated as part of our monitoring and project management engagements.
12 countries covered
International coordination capability across multicentric studies.
Partnerships with 7 global industry leaders
Including Innovative Trials, Occlutech, ICON, Precision for Medicine, Abbott, IQVIA, and Orthofix.
Phase I to IV
Experience spanning the full clinical development cycle, across therapeutic areas.
Why choose Keena as your Clinical Operations partner?
Real flexibility
One-off reinforcement or long-term support, based on your workload.
Methodological rigor
Aligned with ICH GCP standards and Good Clinical Practice.
Tailored approach
Adapted to each protocol, each molecule and each device.
By choosing Keena Life Sciences as your Clinical Operations partner, you gain an operational team from the launch of your study, able to strengthen your teams in FSP mode or take on some or all of your clinical activities. Whether you need one-off CRA reinforcement or full project management, our team adapts to your timeline and your quality requirements.
Facing an activity peak or a need for clinical reinforcement?
Let's talk about your project with our team.
Get in touch