Research Support Technician
Offer DescriptionACADEMIC DEGREEDegree + official master (Justification must be provided with the application).FUNCTIONSSupport to the processes that affect the execution of clinical trials and their quality control:
o Coordination and comprehensive planning of patient and monitor schedules.
o Monitoring of the quality system
o Participation in the medication management process.
o Participation in the preparation and shipment of clinical trial patient samples.
o Management of the warehouse of materials necessary for the execution of trials.RequirementsResearch Field All Education Level Master Degree or equivalentSkills/QualificationsEXPERIENCE
Experience as a research support technician in early phase clinical trial units.
Experience as a user/manager of quality systems in the field of clinical trials.
Experience in the use of Clinical Trials Management Systems (CTMS).OTHERS
Training in the field of clinical trials (good clinical practice in clinical research, IATA,
etc.).Specific RequirementsACADEMIC DEGREEDegree + official master (Justification must be provided with the application).OTHERS REQUIREMENTSEnglish level B2 (Justification must be provided with the application).Languages ENGLISH Level GoodAdditional InformationBenefitsANNUAL GROSS SALARY26.066,88 € without prejudice to the basic update established in state legislation for 2024.Eligibility criteria Experience as a research support technician in early phase clinical trial units. MAXIMUM 30
Experience as a user/manager of quality systems in the field of clinical trials. MAXIMUM 10
Experience in the use of Clinical Trials Management Systems (CTMS). MAXIMUM 10
Training in the field of clinical trials (good clinical practice in clinical research, IATA, etc.). MAXIMUM 10Selection processSELECTION PROCESS STAGES
1. Admission of applications.
2. Competition phase.
3. Interview pase: maximum number of candidates to be interviewed: 3. Minimum score for this
phase: 40.
4. Report of the Tribunal.
5. Resolution.
Note: in order for candidates to be considered for recruitment and employment exchange
purposes, they must have a total score of at least 30 points.SELECTION BOARD
President: Mª Blanca Sánchez Santiago, head of the Valdecilla Clinical Trials Unit and Principal Investigator of
the Project.
Member: Francisco Galo Peralta, IDIVAL Management Director.
Member and secretary: Maria José Marín Vidalled, Coordinator of IDIVAL’s Technological Services.Website for additional job detailsWork Location(s)Number of offers available 1 Company/Institute IDIVAL Country Spain State/Province Cantabria City Santander Postal Code 39011 Street C/ Cardenal Herrera Oria, s/nWhere to apply WebsiteContact State/ProvinceCantabria CitySantander WebsiteStreetC/ Cardenal Herrera Oria, s/n Postal Code39011STATUS: EXPIRED
€26066.88 per year
Santander, Cantabria
Fri, 19 Apr 2024 23:27:49 GMT
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