Job title:
Research Support Technician
Company:
Job description
Offer DescriptionACADEMIC DEGREE
- Medical Specialist in Clinical Pharmacology/Equivalent (must be provided with the
application).FUNCTIONS
- Supporting the development of clinical trials throughout their development with the following
tasks:
- Coordination and comprehensive planning of patients’ agendas for their participation in clinical
trials.
- Care for trial subjects in the Valdecilla Clinical Trials Unit, and specifically assistance in
emergency and urgent situations.
- Monitoring of the quality system
- Interlocution with researchers and monitors for the development of clinical trials.
- Supervision of the tasks of drug administration, testing, sending of samples, etc. o Supervision
of the information systems of the clinical trials.
- Supervision of the information systems used in the clinical trials.
Where to apply WebsiteRequirementsResearch Field Medical sciences » Health sciences Education Level PhD or equivalentSkills/QualificationsVALUED MERITS /SKYLLS
EXPERIENCE
– Experience as a clinical trial coordinator
– Experience as investigator-sub-investigator in clinical trials
OTHERS
– Training in the field of clinical trials (good clinical practice in clinical research, clinical
trial monitoring, IATA, etc.).
– Master’s degree in clinical research
– Research (publications and communications at conferences) in the field of clinical
pharmacology.Specific RequirementsEXCLUSIVE REQUIREMENTS: (1)
ACADEMIC DEGREE
- Medical Specialist in Clinical Pharmacology/Equivalent (must be provided with the
application).
OTHERS REQUIREMENTS • Level B2 English (must be provided with the application).Additional InformationBenefitsANNUAL GROSS SALARY
43.852,23€ without prejudice to the basic
update established in state legislation for 2024.Eligibility criteriaVALUATION OF MERITS
Experience as a clinical trial coordinator
MAXIMUM 15
Experience as investigatorsub- investigator in clinical trials
MAXIMUM 10
Training in the field of clinical trials (good clinical practice in clinical research, clinical trial
monitoring, IATA, etc.)
MAXIMUM 10
Training in Emergency Medicine
MAXIMUM 10
Master’s degree in the clinical field
MAXIMUM 5
Research (publications and conference papers) in the field of clinical pharmacology.
MAXIMUM 10Selection processSELECTION PROCESS STAGES (2)1. Admission of applications.
2. Competition phase.
3. Interview pase: maximum number of candidates to be interviewed: 3. Minimum score for this
phase:30
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: Blanca Sánchez Santiago, Head of the Valdecilla Clinical Trials Unit and Principal Investigator of the
Project.
- Member: Marcos López Hoyos, Scientific Director IDIVAL
- 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/ProvinceCANTABRIA CitySANTANDER WebsiteStreetAVD/ CARDENAL HERRERA ORIA S/N Postal Code39011STATUS: EXPIREDShare this page
Expected salary
€43852.23 per year
Location
Santander, Cantabria
Job date
Thu, 13 Mar 2025 02:03:03 GMT
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