FLEXIBLE CLINICAL TRIAL SUPPORT
– tailored to your needs 

Your clinical trial – our unlimited operational support

On demand professional services for clinical research

Camovis offers a comprehensive portfolio designed to conduct clinical trials efficiently and flexibly. We support you across all study phases – from Phase I to IV – as well as in non-interventional studies (NIS).

Our modular system covers all core operational tasks and can be seamlessly expanded beyond study sites (DCT). It provides additional and reinforcing resources wherever needed, helping to accelerate processes and ensure smooth study execution.

Our ambition: to support your project in every operational situation across the entire study process – reliably, scalable, and practice-oriented.


Site Coordination: Coordination of daily study activities – on-site or remote.

Patient Recruitment: Targeted recruitment strategies to attract qualified study participants.

Clinical Operations: Operational study management – planning, monitoring, and documentation.

✅ Data Handling: Secure on time collection and maintenance of your study data – GDPR compliant.

✅ Consulting & Project Training: Expertise in study planning, quality management & training.

✅ Decentralized Clinical Trials: Enable modern, decentralized and digital study concepts for maximized patient-centricity.

Why Camovis?

  • Experience from over 260 studies in more than 70 indications since 2014.

  • Over 350 qualified Research Professionals, deployed flexibly.
  • We operate in Germany, Austria, Switzerland, Spain and beyond– mobile & flexible.
  • Flexible pricing models following your needs – hourly billing or block booking.

1. Inquiry & initial consultation – We understand your goals.
2. Needs analysis & expert selection – Matching suitable Research Professionals.
3. Project launch & implementation – On‑site or remote.
4. Support & reporting – Continuous optimization.

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