We love Sponsors

Sponsor + Camovis = Successfully managing clinical studies.

More control. More quality. More speed for your clinical trials 💥

As a sponsor, you bear overall responsibility for the success of your clinical studies—from planning and execution to quality, timelines, and budget. At the same time, requirements are increasing: complex study protocols, ambitious timelines, resource constraints at CROs and study sites, and a high level of coordination across multiple partners.

A strong partner by your side – complementing your CRO

Camovis supports you precisely where study success is decided—especially in operational execution at study sites. We do not replace your CRO; instead, we strategically complement their work to minimize delays, inefficiencies, and risks across your trial execution.

Our expertise lies where patients, processes, and timelines directly intersect. We stabilize site performance, accelerate critical workflows, and reduce operational risks—from study start-up through recruitment and conduct to close-out. Through seamless integration into existing structures and close collaboration with your CRO, we create transparency, reliable timelines, and consistently high study quality—always with the goal of ensuring shared study success.

Strong in execution, predictable outcomes.

Since 2014, we have been supporting sponsors, CROs, and study sites in the successful conduct of clinical trials. Our team of more than 350 highly qualified professionals operates in Germany, Switzerland, Austria, and beyond—on-site at study sites as well as remotely.

We combine operational services, training, project management, and consulting to measurably relieve sponsors, minimize risks, and deliver studies efficiently, with high quality and on time.

Focused. Reliable. Effective – our services:

🔹 Site coordination: Operational management of study workflows
🔹 Patient recruitment: Targeted identification, pre-screening, and follow-up
🔹 Clinical operations: Study visits, medical assessments, and sample logistics
🔹 Data handling: Data transfer, eCRF entry, query management, and archiving
🔹 DCT services: Home and virtual visits, remote support, patient-centered care
🔹 Project training: Practical, study-focused training for site teams
🔹 Courses: Webinars, e-learning, and in-house training for study coordinators
🔹 Consulting: On-site performance analyses, audit and inspection preparation, and staff coaching

Camovis – your partner for operational excellence and successful study delivery.


WE ARE AT YOUR SITE – anytime, anywhere, effective.

Contact us to learn how we can specifically support your study processes and, together with you and your CRO, achieve optimal results. Email: info@camovis.de