Research Support Technician
Offer DescriptionACADEMIC DEGREEBachelor in health sciences or life sicences + official master/Equivalent (Justification
must be provided with the application).Where to apply WebsiteRequirementsResearch Field Medical sciences » Health sciences Education Level Master Degree or equivalentSkills/QualificationsVALUED MERITS /SKYLLS
FURTHER
Degree in Social Sciences, Degree in Biochemistry, Degree in Pharmacy,
Degree in Biotechnology, Degree in Information Sciences (Documentation),
Degree in Statistics, Degree in Physics or Mathematics or Degree in
Biomedical Engineering.
Master’s degree in biomedical research, public health or epidemiology.
Specific training in database management and statistical analysis: Courses or
certificates in tools such as SPSS, R, STATA or management of scientific
databases.
Knowledge of research methodology: Studies or complementary training in
clinical study design and scientific writing.
Training in project coordination or clinical studies: Courses or certificates on
management and coordination of multicentre projects, preferably in the
health area.
EXPERIENCE
Experience in clinical data collection and processing, database management,
coordination of multicentre studies, bibliographic research, writing scientific
articles, collaboration in research projects, use of statistical analysis tools.
Experience in processing administrative documentation for ethics committees
and clinical research in general.
Experience in research management
LANGUAGES English (Certificates or diplomas must be provided).
OTHERS Good Clinical Practice (GCP) accreditation.Specific RequirementsACADEMIC DEGREE
must be provided with the application).Additional InformationBenefitsANNUAL GROSS SALARY
28.487,38 € without prejudice to the basic
update established in state legislation for
2024.Eligibility criteriaVALUATION OF MERITSDegree in Social Sciences, Degree in Biochemistry, Degree in Pharmacy, Degree in Biotechnology, Degree in Information Sciences (Documentation), Degree in Statistics, Degree in Physics or Mathematics or Degree in Biomedical Engineering.
MAXIMUM 5
Master’s degree in biomedical research, public health or epidemiology.
MAXIMUM 5
Specific training in database management and statistical analysis: Courses or certificates in tools such as SPSS, R, STATA or management of scientific databases
MAXIMUM 5
Knowledge of research methodology: Studies or complementary training in clinical study design and scientific 5writing.
MAXIMUM 10
Training in project coordination or clinical studies: Courses or certificates on management and coordination of multicentre projects, preferably in the health area.MAXIMUM 5
Experience in clinical data collection and processing, database management, coordination of multicentre studies, bibliographic research, writing scientific articles, collaboration in research projects, use of statistical analysis tools
MAXIMUM 5
Experience in processing administrative documentation for ethics committees and clinical research in general.
MAXIMUM 5
Experience in research management
MAXIMUM 5
Supporting document
MAXIMUM 10
Good Clinical Practice (GCP)
accreditation.
MAXIMUM 10Selection processSELECTION PROCESS STAGES1. Admission of applications.
2. Competition phase.
3. Interview pase: maximum number of candidates to be interviewed: 4. Minimum score for this
phase: 50.
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: Jaime Viera Artiles, Principal Investigator
Member: Francisco Galo Peralta, IDIVAL Management Director.
Member and secretary: Maria José Marín Vidalled, Coordinator of IDIVAL’s Technological Services
€28487.38 per year
Santander, Cantabria
Fri, 18 Oct 2024 22:35:59 GMT
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