Clinical Trial Study Coordinator

hace 5 días


Barcelona, España Vall d'Hebron Institut de Recerca A tiempo completo

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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