Clinical Trials Assistant

hace 7 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.**

**SCEI unit**
VHIR offers a temporary position as a **Clinical Trials Assistant **(CTA) within the SCEI unit.**
**JOB DESCRIPTION**

**Education and qualifications**:
**Required: -**

Certificate of Higher Education (CFGS/FPII): preferably within administration area.

**Experience and knowledge**:
**Required: **

Specific training and /or experience in administrative management of clinical trials (CTA)

Good command of MS Office and other computer tools.

Good written and oral communication skills in Catalan, Spanish and English

Personal skills: well-organized, ability to work responsibly and with the ability to work under tight deadlines. Team player
with excellent interpersonal skills.

**Main responsibilities and duties**:

Receive and review all documentation related to requests for ethical evaluation of clinical trials, clinical research or research

projects.

Register (physically and electronically) the specific documentation resulting from the activity of the unit and keep updated

the corresponding records.

Ensure the appropriate implementation of the established administrative procedures, both for the management of data entry

and for its distribution and recording.

Return the assessments resulting from the evaluation of the CEIC to the agents involved in the research projects.

Provide advice to investigators, sponsors and CROs on administrative procedures (requirements, procedures,

Handle all outgoing or incoming correspondence

Telephone assistance to sponsors, CROs and investigators.

Ensure that the activities are carried out in accordance with the requirements established in the procedures of the quality

system of the unit, promoting and implementing the continuous improvement in its field of action.

**Labour conditions**:

Full-time position

Starting date: immediately

Length of the contract: temporary (to cover a leave)

Gross annual salary: 20.716,46 €

**How to apply**:



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