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SERVICES
Flexible. Specialized. Everywhere.

We are at your site

Throughout all phases – whether analog and digital.

Since 2014, Camovis has successfully conducted over 260 clinical trials in accordance with the German Medicines Act (AMG) and the German Medical Devices Act (MPG) in collaboration with customers and partners. This has involved the professional supervision of phase I to IV studies and non-interventional studies (NIS) in over 70 different indications. Since 2021, Camovis has expanded its involvement to include innovative DiPA and DiGA projects, thereby supporting the development of digital health applications.

Flying Research Professionals
Mobile support – anytime, anywhere.

Camovis offers flexible, tailored support for your clinical trials through a network of over 350 qualified Camovis Research Professionals. Whether on site or remotely, by the hour or by the day –we are exactly where your project needs us. Whether for short-term assignments or long-term support, we deliver the highest standards of quality and reliability, fully aligned with your specific requirements, across Germany, Austria, and Switzerland. Other locations are available upon request.

Our services

As flexible as your requirements.

Training Center

Make your teams work.

You choose – we deliver
Qualifications tailored to your needs.

We ensure that Research Professionals with the right expertise are available to you. This way, we not only guarantee seamless integration into your study team, but also the highest level of professionalism and flexibility on site.

 


Starter
Level

  • Has up to one year of experience in clinical research and is ideally suited for projects that require basic support.

Professional
Level

  • Has more than one year of experience, with solid expertise and confident in dealing with study processes

Senior
Level

  • Has more than five years of experience, broad specialist knowledge, and in-depth practical expertise. Numerous years of experience in various projects make Camovis Research Professionals ideal for complex and demanding studies.

Reference projects

This is how we shape change.
Study implementation
AMG phase 1 study for urticaria

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Study support
AMG phase 3 study for hypercholesterolemia

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Study coordination
in everyday clinical care

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Study support
Vaccination studies

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Study coordination
DiPA study

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Study support
Simulation study on self-injections

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Mehr

FAQ – You ask, we answer

Why are Flying Research Professionals needed?
The demand for qualified personnel in clinical trials is increasing, while trial centers often struggle with a lack of resources. In addition, trial timelines can be unpredictable, requiring maximum flexibility in personnel planning. Flying Research Professionals offers mobile, needs-based support to help sites and sponsors conduct studies flexibly, efficiently, and with reduced workload.
Why don't we talk about “Flying Study Nurses” anymore?
Until 2025, we used the term “Flying Study Nurse.” As our services and roles evolved, we changed the name to “Flying Research Professionals.” This new term is more internationally compatible, gender-neutral, and more accurately reflects our expanded range of expertise in clinical research. Camovis employs specialists from a wide range of backgrounds—including Study Nurses, Study Coordinators, medical documenters, Clinical Research Associates (CRAs), principal investigators, and project managers. Together, they bring their expertise across a wide variety of roles, ensuring the success of clinical trials with flexibility, commitment, and professionalism.
How does Camovis work?
Camovis offers tailor-made solutions for conducting clinical trials and supporting trial centers. The company provides qualified personnel, known as Flying Research Professionals, on a temporary basis. These professionals are flexible and mobile, taking on tasks that cannot be covered by the study team. The location, time period, and area of application are completely flexible. Thanks to an extensive database of numerous Flying Research Professionals with varying levels of experience and expertise, Camovis can respond flexibly to needs and provide optimal support for study processes.
Who uses our services?

Camovis works with a wide range of stakeholders in clinical research and development. Our customers and partners include sponsors (pharmaceutical and biotech companies), contract research organizations (CROs), and study sites in hospitals and medical practices. Camovis offers these and other organizations customized solutions that are flexibly tailored to the individual requirements and challenges of each clinical trial.

Which projects are supported?
Camovis supports clinical trials in all phases, from Phase 1 to Phase 4, as well as non-interventional studies (NIS). We have extensive experience with clinical trials under the German Medicines Act (AMG), the German Medical Devices Act (MPG), as well as in projects relating to digital care applications (DiPA) and digital health applications (DiGA). Through our work in study projects with over 70 different indications, we have developed broad practical expertise and can reliably support the implementation of studies in a wide range of areas.
Which locations are supported?

Camovis primarily operates in Germany, Switzerland, and Austria. Thanks to our mobile readiness, we can flexibly cover not only larger cities but also smaller towns in order to meet the specific needs of each clinical trial.

How quickly can I start a project with Camovis?

Camovis can usually begin supporting your project on site within two weeks.
The start date depends on various factors, including the duration of the assignment, the number of Flying Research Professionals required, their necessary qualifications, and the specific tasks to be. As demand is high and we always want to offer the best possible service, we recommend involving Camovis as early as possible to guarantee the availability of the necessary resources for the project.

How expensive is a Flying Research Professional?
The cost of a Flying Research Professional depends on various factors, such as the number of hours required, the tasks to be performed, and the experience of the professional. There is the option of hourly billing or a more affordable quota booking for longer assignments. The exact costs vary depending on the specific requirements of the project.

The use of Flying Research Professionals is beneficial for all study participants, as faster recruitment, accelerated study execution, and increased data quality can relieve the study team at critical points and improve the study results.

What pricing models are available?

Camovis offers a range of flexible pricing models. The hourly billing model is ideal for variable or short-term assignments, where bookings and cancellations can be made at any time. It is particularly suitable for projects with unpredictable workloads or changing requirements. The quota model, on the other hand, involves booking pre-agreed service volumes, with the hourly rate being lower than with hourly billing. This model is particularly advantageous for longer-term, easily plannable, or regular assignments.

What training do Flying Research Professionals have?

Camovis Flying Research Professionals typically have a medical or scientific background with relevant training or education, often in fields such as nursing, biology, and related disciplines. Some also have experience as Clinical Research Associates (CRAs). All Research Professionals are ICH/GCP-trained to ensure the highest standards in the conduct of clinical trials. For each project, we carefully handpick the Research Professionals to perfectly match its specific requirements.

How are Flying Research Professionals selected for a project?
For each project, Camovis selects the Research Professionals based on the specific requirements of the test center and the project. We take into account both the professional qualifications and previous experience of the Research Professionals in similar studies or projects.
In addition, we value soft skills such as communication, teamwork, and organizational abilities to ensure they can meet the demands of day-to-day study operations.
How are Flying Research Professionals prepared for new projects?

Before the start of a project, all Flying Research Professionals undergo preparatory training that is specifically tailored to the project in question. Their existing qualifications and skills are carefully assessed and, if necessary, supplemented with additional training. This ensures that they are optimally prepared for the specific challenges and can quickly get started with the practical project work.

How is data protection ensured?
Patient data and study data are highly sensitive, and Camovis is committed to their strict protection. Data protection is regulated by a separate data processing agreement between Camovis and the trial center in accordance with the GDPR. Access to patient records and the processing of patient data are carried out exclusively in accordance with the applicable data protection guidelines and labor law requirements in order to guarantee the confidentiality and security of the data at all times.
How is quality ensured?

Quality is ensured through comprehensive ICH/GCP training and regular quality assurance checks. Every Flying Research Professional is specifically prepared for the specific requirements of the respective study. In addition, work processes are continuously monitored and controlled, taking into account feedback from both trial centers and sponsors, in order to guarantee the highest standards in the conduct of clinical trials.

Would you like some support?

Book your Flying Research Professional now
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