Research Support Technician
Offer DescriptionACADEMIC DEGREE
Degree + oficial master/equivalente (Justification must be provided with the application).FUNCTIONS
To monitor the activities of the clinical research project carried out in the assigned centres as defined by
the project manager.
-Ensure effective communication between the research team/promoter in the centres assigned to him/her.
To carry out the start-up visit and train the research team in the activities of the project.
-To carry out the monitoring in compliance with the Monitoring Plan and manual,
-Verify that the protocol and its modifications are complied with.
-Ensure compliance with Good Clinical Practice standards, applicable legislation and Standard Operating
Procedures.
-Performing the clinical research project closure visit.
-Prepare the Monitoring and Review Reports to the project manager/promoter.
-Keep the essential project documentation updated and correctly filed in the centres assigned to him/her.
-To carry out external monitoring in centres participating in the clinical trials of the platform.
-Support for the resolution of inconsistencies, deviations and errors in the data collected from the trial
(queries).
-Ensure traceability of medication delivered to assigned sites.
-Maintain the information required from the assigned sites in the project monitoring tools.
-Actively collaborate in the quality assurance of the data, documentation and processes of the assigned
centres.
-Support to the Project Manager in those activities required for the proper development of the project.
Support the Head of Pharmacovigilance and/or the Project Manager in the follow-up of reported RAGI, AAG,
RAG or AAs.– Perform expedited reporting of suspected unexpected serious adverse reactions (SUSARs) from clinical
trials.
– Produce periodic safety reports on clinical trials.
– Follow-up on any safety issues that may occur with investigational medicinal products or medical devices.Where to apply WebsiteRequirementsResearch Field Medical sciences » Health sciences Education Level Master Degree or equivalentSkills/QualificationsVALUED MERITS /SKYLLS
FURTHER
-Specialisation in Clinical Pharmacology
-Training in Pharmacovigilance
-Certification in Good Clinical Practice
EXPERIENCE
-Experience in the monitoring of Clinical Trials.
-Experience as Data Manager or Study Coordinator in Clinical Trials.
LANGUAGES -English
OTHERS -Availability for external monitoringSpecific RequirementsEXCLUSIVE REQUIREMENTS:
ACADEMIC DEGREE
Degree + oficial master/equivalente (Justification must be provided with the
application).Additional InformationBenefitsANNUAL GROSS SALARY DURATION OF THE CONTRACT
22.351, 43 € without prejudice to the basic
update established in state legislation for 2024Eligibility criteriaVALUATION OF MERITSSpecialisation in Clinical Pharmacology
MAXIMUN 20
Training in PharmacovigilanceMAXIMUN 10
Certification in Good Clinical Practice
MAXIMUN 5
Experience in the monitoring of Clinical Trials.
MAXIMUN 10
Experience as Data Manager or Study Coordinator in Clinical Trials.
MAXIMUN 5
English
MAXIMUN 5
Availability for external monitoring
MAXIMUN 5Selection processRECRUITMENT INFORMATION
SELECTION PROCESS STAGES1. Admission of applications.
2. Competition phase.
3. Interview pase: maximum number of candidates to be interviewed:4. Minimum score for this
phase: 10.
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: María del Mar García Saiz, Principal Investigator.
Member: Francisco Galo Peralta, IDIVAL Management Director.
Member and secretary: Maria José Marín Vidalled, Coordinator of IDIVAL’s Technological Services
Santander, Cantabria
Mon, 26 Aug 2024 04:41:11 GMT
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