Clinical Trial Study Coordinator
hace 5 días
VHIR-RRHH-FOR-003_vs01 _
The Vall d'Hebron Research
Institute (VHIR) is a public sector
institution that promotes and
develops the research, innovation
and biosanitary teaching of the
Vall d’Hebron University Hospital.
Through the excellence of our
research, we identify and apply
new solutions to the health
problems of society and we
contribute to spread them around
the world.
In April 2015, the **Vall d’Hebron**
**Research Institute (VHIR)** obtained
the recognition of the European
Commission **HR Excellence.**
This recognition proves that VHIR
endorses the general principles of **the**
**European Charter for Researchers**
**and a Code of Conduct for the**
**Recruitment of Researchers**
**(Charter & Code)**.
Thus, there are no restrictions of
gender, national origin, race, religion,
sexual orientation or age and
**strongly encouraged to apply.**
**Clinical Trial Study Coordinator**
**Multiple Sclerosis Centre of Catalonia-VHIR**
VHIR offers vacancy/vacant position for a coordination of clinical trials within the Neuroimmunology research group - Multiple
Sclerosis (MS) Centre of Catalonia
The main objectives of the Clinical Neuroimmunology Group through research are to improve the quality of life of multiple
sclerosis (MS) patients and attain a greater understanding of the pathogenic mechanisms, aiming to develop new and more
effective therapeutic means. Other interests in research are: therapeutic tools in MS; disease susceptibility, diagnostic and
prognostic markers in MS; study of the response to treatment in MS patients; clinical and radiological study of primary
- progressive MS; epidemiology of MS; and patient-oriented outcomes.
**JOB DESCRIPTION**
**Education and qualifications**:
**Required: **
Degree in health science or related field
Good spoken and written English
**Desired:
Ability to work autonomously and in team with different professionals in the center (MDs, nurses, etc)
Problem solving
Proactive attitude***
**Experience and knowledge**:
**Required: **
Experience in coordination of clinical trials
English is mandatory
**Main responsibilities and duties**:
- CRF data entry
- Sample processing and shipment
**Labour conditions**:
- Indefinite Contract
- Full-time position (40h/week)
- Gross salary per year: 22.000€ / 24.000€
- Incorporation: immediate
**What can we offer? -**
Skillful and social colleagues in a dynamic environment.
- Challenging tasks and a wide range of responsibilities.
- Personal training opportunities.
- Flexible working hours.
- 23 days of holidays + 9 personal days.
- Flexible Remuneration Program (including dining checks, health insurance, transportation and more).
- Annual teambuilding events.
- **How to apply**:
Applicants should submit a full Curriculum Vitae and a presentation letter with reference to Mrs. Silvia Ferrer, Head of HR
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