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Some job offer, PDF Print E-mail
---Procedencia: 
 Institución:Institut d'Investigacio 
Biomedica de Bellvitge (IDIBELL) 
 Contacto correo-e:
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---
Reference: 196_SS_VR

IDIBELL is looking
 for a Study Coordinator
 for Cancer Clinical Trials

 

About the research group

ICO-L’Hospitalet is a reference hospital 
for the clinical research in cancer. 
Their two units (UIC and UFF1) have been
 participating in 507 clinical trials with active 
recruitment or with current activities 
during 2020 and 874 patients decided 
to participate in them. Many of these trials 
are testing the most promising therapies
 in cancer and investigators involved 
in them are specialized and up-to-date 
with the latest advances in new treatments. 
UIC and UFF1 units they are 
the best professionals who carry out 
the most demanding clinical trials



About the role

Coordination of Oncology Clinical Trials
 ( Solid Tumour neoplasms ) 
into Clinical Research unit 
for advanced phase trials.
Performance and application 
of coordinated procedures 
between the different clinical 
services involved in the inclusion, 
treatment and follow-up 
of patient’s participation.
Support to Investigators 
and electronic 
tools implementation.
Management of human tissues
 between different external
 referring sites.
Record of transactions 
in sponsor’s systems (IWR). 
Record of trial and patient’s 
information into clinical 
and research applications.
Administrative procedures 
during the study
SAE completion
Case Report Form training, 
completion and correction. 
Queries resolution.
Communication with Sponsors 
and CROs.
Preparation and attention 
to monitoring visits, audits 
and inspections, internal 
and external information
 meetings.
  

Job requirements

Professional experience

At minimum of 6 months 
of experience in oncology 
or hematology cancer
 clinical trials ( as coordinator 
or data entry.
Coordination or data entry 
in phase I, II and 
III cancer trials.
Education and training

Education: Bachelor degree
 in life Science.
Education In clinical trials 
and clinical research.
Education in 
Good Clinical Practices.
Technical skills 

Office (Outlook, Excel, Word),
 internet, patient’s files.
Internet Browsers (Firefox, 
Chrome, Edge) 
and patient’s files.
Languages

 Good command 
of the English language.
 

We will value, but not required

Experience as Clinical trials Monitor.
Familiarity with SAP Argos Electronic 
Medical Record system.
Previous experience in data 
management of oncology studies.
Previous experience in clinical trials 
(other than cancer).
 

What do we offer

Nº of positions: 1
Start date: December 2021
Contract duration: Temporary
Estimated annual gross salary: 
it is commensurate 
with qualifications 
and consistent with 
our pay ranges.
You will be part 
of a multicultural team.
 We have a fun loving and 
friendly international work 
environment.
Flexible working schedule - 
We know you have a life outside 
of work and we will work with you 
to make sure it's kept that way.
Benefits of constant training
 are offered.
We offer and promote diverse 
and inclusive conditions. 
Applicants are made free 
from any discrimination.


Selection process

Pre-selection: The pre-selection 
process will consist on an eligibility 
check based on qualifications 
and expertise reflected 
on the candidate's CV.
Interview: Best positioned, 
pre-selected candidates 
may be called to arrange an interview. 
Candidates will be interviewed 
by the hiring manager 
and an ad hoc selection panel.
Formal offer letter: Once identified,
 the People Management Unit will send 
a job offer to the successful candidate 
indicating start date, salary, working 
conditions, and any additional 
relevant details.
 

Deadline: Please submit
 your application by 22 November 2021.

 

Data protection notice

IDIBELL ensures that applicants’ personal 
data are processed as required 
by the EU General Data Protection Regulation 
(GDPR) and Spanish Law 3/2018 
on Data Protection. Personal data is
 processed solely for the purpose 
of the selection procedure.

 

Our institute

IDIBELL is a research center that integrates 
the biomedical research of the Bellvitge 
University Hospital (HUB), the Catalan 
Institute of Oncology (ICO), 
and the University of Barcelona
 in the Bellvitge Campus (UB), 
and the Viladecans Hospital (HV). 
The research focuses
 of IDIBELL are cancer, neuroscience, 
translational medicine and regenerative
 medicine. Research, innovation
 and society are the pivots on which 
researchers work every day in order
 to improve the quality of life of citizens.

 

Observations

The 'HR Excellence in Research' award 
represents IDIBELL’s commitment 
to the implementation of Human Resources
 policies, which oversee the attracting 
and development of talent in an open, 
transparent, and based on personal merit,
 in alignment with the principles 
of the European Charter 
for Researchers and the Code 
of Conduct for the Recruitment 
Researchers (Charter and Code).

IDIBELL is committed to the principles 
of the Code of Conduct for the Recruitment 
of Researchers of the European Commission
 and the implementation of open, 
transparent and merit-based 
recruitment (OTMR).

 
Some job offers, PDF Print E-mail
Procedencia: 
 Institución:Hospital Clínic - 
Universidad de Barcelona
 Contacto 
correo-e:
 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
---
El grupo de Investigación Muscular 
y Función Mitocondrial del Hospital
 Clínic de Barcelona busca candidatos 
para la solicitud de becas competitivas  
para el desarrollo de investigación 
biomédica. Por este motivo es 
imprescindible disponer de nota 
de expediente académico igual 
o superior a 8. Se valorará 
asimismo disponer 
de un máster oficial. 
El proyecto en el que 
se involucraría el candidato 
es un proyecto relacionado 
con las enfermedades minoritarias 
de tipo obstétrico, para la búsqueda 
de nuevos biomarcadores 
y/o opciones terapéuticas. 
La investigación que llevará 
a cabo el candidato estará 
centrada en dos objetivos f
undamentales:
•	Establecer la huella de 
microRNAs y el perfil transcriptómico
 característico del crecimiento 
intrauterino restringido tanto 
en pacientes como en un 
modelo animal.
•	Evaluar la modulación 
de la afectación molecular, 
cardiomiocinas y la bioenergética
 en función de la dieta ingerida.
Se ofrece la oportunidad de entrar 
de lleno en el campo de la
 investigación biomédica 
y el desarrollo de una tesis doctoral.
 El candidato participará activamente 
en un proyecto de investigación y 
en el desarrollo de todas las tareas 
relacionadas con el diseño y la 
realización de experimentos,
 así como, en la difusión y 
divulgación de resultados y
 la redacción de manuscritos 
originales.
Los candidatos interesados 
pueden contactar con 
nosotros a través de 
la siguiente dirección 
de correo electrónico:
Dra. Glòria Garrabou: 

 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
Dr. Francesc J. García:
 
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 ----------------
Información complementaria 
de la oferta:
Los interesados pueden 
enviar su CV y carta de 
motivación a las siguientes 
direcciones de correo electrónico:

Dra. Glòria Garrabou: 

 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
Dr. Francesc J. García: 

 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
 
Some job offers, PDF Print E-mail
--Procedencia: 
 Institución:Centro de Investigaciones Biologicas Margarita Salas, CSIC
 Contacto correo-e:
 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
---
Se busca técnico de laboratorio para integrarse en el grupo de Biología 
Celular de Aspergillus.
El/la candidato/a se incorporaría al grupo para realizar funciones 
generales de mantenimiento de cepas del hongo, medios de cultivo 
y soluciones de uso general del laboratorio. Además aprendería
 a generar cepas modificadas del hongo que servirán para
 la observación por microscopía de fluorescencia. Para ello se 
precisa de conocimiento en aislamiento de ADN, manipulación
 y análisis por electroforesis, y conocimiento de técnicas 
generales de biologia molecular.
 

 ----------------
Información complementaria de la oferta:
Los requisitos de los candidatos son los siguientes:

1. Estar inscritos en el Fichero del Sistema Nacional de Garantía Juvenil
 en la fecha de la firma del contrato y estar en situación de beneficiarios 
en dicho fichero en esa fecha
2. No estar vinculados laboralmente con la institución que les contrate
 en la fecha de publicación de esta convocatoria en el Boletín Oficial 
de la Comunidad de Madrid.
3. Estar en posesión de la titulación exigida en la fecha de firma 
del contrato. 

Perfil requerido. 
Técnico Superior en Laboratorio de Análisis y de Control de Calidad
 o Técnico Superior en Laboratorio Clínico y Biomédico.

Información y contacto para envio de CVs: Eduardo A Espeso, 
CIB Margarita Salas, Ramiro de Maeztu, 9, lab 247,
 
 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
 
Some job offers, PDF Print E-mail
---Procedencia: 
 Institución:Fundación para la Invesigación Biomédica del H. U. La Paz
 Contacto correo-e:
 This e-mail address is being protected from spambots. You need JavaScript enabled to view it
 
---
Job Functions:
•	Project management of a multicentre European Project focused 
on Paediatric Transplantation
•	Budget and contract control for the project
•	Development of European economic reporting
•	Development of deliverables and reports related to the project 
work packages
•	Support of the research studies in the different centres
•	Monitoring of project activities and working groups
•	Technical and administrative support of the centres 
in their activities and tasks
•	Continuous relationship with the participating centres
 and the personnel in charge
 of the different work packages of the project
•	Organization and participation in coordination and 
update meetings with project members
•	Control of compliance with the tasks and objectives 
established in each of the centres

Skills, Experience and Qualifications required:
•	Graduate or master's degree in Business Administration 
with management experience
•	Previous experience (of at least 2 years) In project 
management is valued
•	Knowledge or experience in the healthcare sector 
or in clinical research
•	Knowledge or experience in handling patient data 
/ European registries / electronic health 
records is valued
•	Good ability to manage project budgets
•	Experience in administrative management 
of documentation
•	Excellent organization and multitasking work
•	Ability to write documentation and make 
periodic reports
•	Professional use of Microsoft Office package
•	Good at coordinating activities and organizing 
tasks
•	Teamwork skills and proactive personality
•	Essential: spoken and written fluency 
in English
•	Strong communication skills in English 
and Spanish
•	Ability to travel up to 20% time


 ----------------
Información complementaria de la oferta:
The selection interview will be in English.
 
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