Research Nurse - 60% to 80%

Job criteria

• Professions :
• Clinical Research Nurse (M/F)
• Min experience :
• 3 to 5 years
• Degrees :
• Bachelor / HES
• Skills :
• English
• Locations :
• Genève
• Conditions :
• Permanent
• Salary not specified
• Part-time

Job criteria

• Professions :
• Clinical Research Nurse (M/F)
• Min experience :
• 3 to 5 years
• Degrees :
• Bachelor / HES
• Skills :
• English
• Locations :
• Genève
• Conditions :
• Permanent
• Salary not specified
• Part-time

The company : HUG ##

With more than 13'000 employees representing 160 professions, the Hôpitaux Universitaires de Genève are a reference institution at national and international levels. To learn more about our institution, take a few minutes to consult our 2025 retrospective by clicking here.

The Geneva Translational Research in Infections and Vaccination (GeTRIV) platform is a joint project of the Faculté de médecine and the HUG, led by the Centre des maladies virales émergentes (CMVE) and vaccinologie as well as by the VIH research unit. Its objective is to promote translational science in the field of immunovirology and vaccinology, by providing state-of-the-art laboratories, biobank facilities as well as shared offices and meeting spaces intended to welcome clinicians and fundamental researchers, in order to bridge the gap between fundamental research and clinical applications.

The GeTRIV is recruiting a clinical research nurse to work within its team on all projects conducted within the GeTRIV.

More info on HUG

Job description ##

You participate in studies conducted at GeTRIV. You work mainly in the Bâtiment de la Tulipe (64, avenue de la Roseraie). Home visits or sampling in other hospitals in the canton of Genève are also possible.

As part of the studies, you participate in identifying eligible participants and verify inclusion criteria in collaboration with the study investigators. You apply the current protocols, participate in meetings, use monitoring tools and contribute to the training of the different stakeholders involved in the participants' journey.

You welcome, take charge of, and accompany the participants of the various studies. You ensure their good understanding of the information transmitted and participate in completing it if necessary. You organize, plan, and carry out the various visits provided for by the study, notably inclusion, follow-up, and end-of-study visits.

You perform the paramedical acts required by the protocol, and coordinate the transfer of samples with the laboratories at GeTRIV and at HUG. You also guarantee the traceability of the different stages in accordance with the protocol requirements.

Finally, you enter data into the study databases, will verify their accuracy and consistency, and ensure the management of documentation as well as treatments related to the studies, in collaboration with the GeTRIV team. You work mainly during regular weekday hours. Work on weekends or in the evening / at night may occasionally be considered, according to terms to be agreed upon, with recovery during the week, according to the needs of the different studies.

Profile description ##

You hold a Bachelor HES in nursing or a title deemed equivalent recognized and registered by the Croix-Rouge Suisse, and you are proficient in IT tools as well as the electronic patient record (DPI).

You have a very good sense of organization and are comfortable in an environment requiring transversal work and collaboration with different professionals.

Theoretical and practical knowledge in the field of clinical research is an asset. A good command of English, both spoken and written, is also a plus.