Clinical Research Nurse - JYF1117

The Clinical Research Nurse will : Assist the investigator and the medical team in all stages of the study (patient recruitment, informed consent, data collection, filling in the case report forms (CRFs)); Carry out the services stated in the study protocol and more particularly clinical procedures; Be capable of carrying out medical procedures if needed; Organise the research protocol and participate in managing the collected data.
1A-B, rue Thomas Edison, Strassen 1445, Luxembourg
01/12/2017 11:36:17
              Key Accountabilities
              Participate in recruiting participants as well as obtaining their informed consent, organising meetings and participating in other associated actions.
              Perform the nursing procedures and medical procedures (drawing blood, sampling) mentioned in the protocol for each participant in the study.
              Transfer the biological samples to the laboratories concerned within the periods defined in the protocol and as per the conditions required by the study.
              Collect the results of the analyses and file the documents in the case files of each participant.
              Participate in preparing the study case files and worksheets.
              Collect data directly in the hospitals using hospitalisation case files.
              Enter the collected data in the input tools specific to the project and in strict compliance with the CRF filling recommendations.
              Manage the equipment required for the study and tidy up the rooms after they are used.
              Participate in meetings related to the research project (study meetings), internal meetings (team meetings) and external meetings (sponsor meetings: initiation, monitoring, etc.).
              Participate in drafting the documents needed for the project and for classifying the case files.
              Check the consistency of the collected data and ensure the management of data queries.
              Monitor the data concerning the safety of the participants (Safety Data).

              Nursing degree authorising work in Luxembourg.
              Must have professional experience of at least 2 years in a nursing job in a hospital or healthcare network.  (Experience in clinical research, emergency/resuscitation services and/or oncology would be an added advantage).
              Must have good interpersonal and negotiation skills, precision in work and organisational skills.
              IT skills: Word, Excel, IE, Outlook Express, PowerPoint.
              Language skills: German, Luxembourgish, French and English are required. Portuguese is considered an asset.

              REF.: CM/CRN1117/JYF/CIEC
              CDI - Full time - Available immediately