Job title:
Research Support Technician
Company:
Job description
Offer DescriptionACADEMIC DEGREEDegree in biomedical sciences + oficial master/equivalent (Justification must beprovided with the application).EXPERIENCEWork experience in basic research/laboratory (Justification must be provided with theapplication).OTHERS REQUIREMENTSGood clinical practices course in force (Justification must be provided with theapplication).FUNCTIONSCoordination of clinical trials in the area of liver and inflammatory diseases. Data collection and registrationin databases.RequirementsResearch Field Medical sciences » Health sciences Education Level Master Degree or equivalentSkills/QualificationsVALUED MERITS /SKYLLSFURTHER -Academic record (Grade point average ≥ 7.0/10)-Complementary related training (i.e., courses, internships, trainings…).EXPERIENCE-Clinical trial coordination experience of more than 3 years.-Data collection, analysis and reporting according to study protocols and industrystandard.-Preparation of documents for the ethics committee and passing full audits and siteinspections.-Performing laboratory techniquesLANGUAGES -English (Certificates or diplomas must be provided).OTHERS -Participation in research projects and/or scientific publications.Specific RequirementsEXCLUSIVE REQUIREMENTS: (1)ACADEMIC DEGREE Degree in biomedical sciences + oficial master/equivalent (Justification must beprovided with the application).EXPERIENCE Work experience in basic research/laboratory (Justification must be provided with theapplication).OTHERS REQUIREMENTS Good clinical practices course in force (Justification must be provided with theapplication).Languages ENGLISHResearch Field Medical sciences » Health sciencesAdditional InformationBenefits29.790,72 € without prejudice to the basicupdate established in state legislation for2024.Indefinite (linked to the duration of the project or to externalfinancing or financing from public grants in full competition).Eligibility criteriaVALUATION OF MERITSMERITSAcademic record (Grade point average ≥ 7.0/10) MAXIMUN 10Complementary related training (i.e., courses, internships, trainings…).MAXIMUN 15Clinical trial coordination experience of more than 3 years. MAXIMUN 15Data collection, analysis and reporting according to study protocols and industry standard. MAXIMUN 10Preparation of documents for the ethics committee and passing full audits and site inspections.MAXIMUN 5– Performing laboratory techniques MAXIMUN 5English Certificate Level-B1: 2 points-B2 or more: 5 pointsParticipation in research projects and/or scientific publications. MAXIMUN 5Selection processSELECTION PROCESS STAGES1. Admission of applications.2. Competition phase.3. Interview pase: Minimum score for this phase: 404. Report of the Tribunal.5. Resolution.Note: in order for candidates to be considered for recruitment and employment exchangepurposes, they must have a total score of at least 30 points.SELECTION BOARD
- President: Javier Crespo García, principal investigator
- 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/ProvinceSent for Approval CitySANTANDER WebsiteStreetC/ Cardenal Herrera Oria, s/n Postal Code39011STATUS: EXPIRED
Expected salary
Location
Santander, Cantabria
Job date
Wed, 15 May 2024 03:20:57 GMT
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