Research Support Technician

Job title:

Research Support Technician

Company:

Job description

Offer DescriptionACADEMIC DEGREE

• Bachelor in health sciences or life sicences + official master/Equivalent (Justification

must be provided with the application).FUNCTIONS
For the position of Research Support Technician, key functions include the comprehensive management of
the databases associated with the CRAIS study, ensuring the correct collection, storage and analysis of
data. In addition, you will coordinate the participating centres, ensuring efficient communication and
compliance with the project objectives. Within the research tasks, an exhaustive bibliographic search will
be carried out to keep the relevant scientific references and advances up to date, as well as the writing of
research articles for the dissemination of the results. You will also actively participate in the coordination of other studies carried out by the rhinology section within the otorhinolaryngology service of the Marqués de
Valdecilla University Hospital, collaborating with the research team in the design and execution of scientific
projects.
Her activities will include:
– Management of legal documentation, agreements, contracts, etc.
– Administrative management.
– Monitoring the progress of the project, liaising with researchers from different centres.
– Advising researchers on study monitoring.
– Preparation of the necessary monitoring documentation (technical reports, budgets, etc.).
– Preparation of documentation for justification and, where appropriate, auditing.
– Dissemination of the most important aspects of the project.
– Support in all tasks related to the coordination of the CRAIS project.Where to apply WebsiteRequirementsResearch Field Medical sciences » Health sciences Education Level Bachelor 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.
LANGUAGES  English (Certificates or diplomas must be provided).
OTHERS  Good Clinical Practice (GCP) accreditation.Specific RequirementsBachelor in health sciences or life sicences + official master/Equivalent (Justification
must be provided with the application).
EXPERIENCE

• Experience in research management (Justification must be provided with the application).

Additional InformationBenefitsANNUAL GROSS SALARY DURATION OF THE CONTRACT
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. Supporting document
MAXIMUN 5
Master’s degree in biomedical research, public health or epidemiology.
Supporting document
MAXIMUN 5
Specific training in database management and statistical analysis: Courses or certificates in tools such as SPSS, R, STATA or management of scientific databases
MAXIMUN 5
Knowledge of research methodology: Studies or complementary training in clinical study design and scientific 5writing.
MAXIMUN 10
Training in project coordination or clinical studies: Courses or certificates on management and coordination of multicentre projects, preferably in the health area. Supporting document
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
MAXIMUN 5
Experience in processing administrative documentation for ethics committees and clinical research in general.
MAXIMUN 5
English
MAXIMUN
10
Good Clinical Practice (GCP) accreditation.
MAXIMUN 10Selection processRECRUITMENT INFORMATION
SELECTION PROCESS STAGES
1. 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.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/n GeofieldContact State/ProvinceSent for Approval CitySANTANDER WebsiteStreetC/ Cardenal Herrera Oria, s/n Postal Code39011STATUS: EXPIREDShare this page

Expected salary

Location

Santander, Cantabria

Job date

Thu, 03 Oct 2024 00:02:24 GMT

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