Clinical Trial Data Base Manager - Barcelona, España - Vall d'Hebron Institut de Recerca

Vall d'Hebron Institut de Recerca

Empresa verificada

Barcelona, España

hace 2 semanas

Publicado por:

Isabel García

beBee Recruiter

Descripción

VHIR-RRHH-FOR-003_vs01_

TheVall 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

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).

VHIR embraces Equality and

Diversity. As reflected in our values

we work toward ensuring inclusion

and equal opportunity in

recruitment, hiring, training, and

management for all staff within the

organization, regardless of gender,

civil status, family status, sexual

orientation, religion, age, disability

or race.

Clinical Trial Data Base Manager

Clinical Trial Management Unit
The Clinical Trials Management Unit is responsible for follow-up the execution of commercial clinical studies

at the Vall d'Hebron Campus.

The primary objective of this Unit is to contribute to the consolidation of the Vall d'Hebron University Hospital

as an international clinical trial reference center, through the implementation of a new management model for

clinical trials at Vall d'Hebron Campus. A management model that aims to ensure quality in clinical trials that

generates opportunities for those researchers on campus, using the latest technology available to treat their

patients, and improve their quality of life
_._
The Clinical Trial Management Unit wants to incorporate a Clinical Trial Data Base Manager.

JOB DESCRIPTION

Education and qualifications:

Required:

PhD in Science
Advanced Microsoft office skills
Fluency in Catalan, Spanish, English (business level)

Desired:

Master in Clinical Trials or similar program
Training in Good Clinical Practice (GCP) and clinical trials methodology.
VHIR-RRHHFOR003_vs01_

TheVall 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

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).

VHIR embraces Equality and

Diversity. As reflected in our values

we work toward ensuring inclusion

and equal opportunity in

recruitment, hiring, training, and

management for all staff within the

organization, regardless of gender,

civil status, family status, sexual

orientation, religion, age, disability

or race.

Experience and knowledge:

Required:

At least 5 years of experience working in hospital environment and research database
Advanced data mining skills
Ability to work independently as well as in a team environment
Good communication and team player skills

Desired:

Knowledge of Clinical Trial Management Systems and Dashboards
Organized and methodological person with high motivation and initiative

Main responsibilities and duties:

Manage and keep up to date the Vall d'Hebron Research Institute clinical trial database.
Give support to the team cleaning the database (CTMS) to guarantee a reliable information
Draft the CTMS guidelines with the units involved in the use of the systems.
Prepare/Organize in collaboration with the Clinical Trial Management Unit activities for the implementation of

the CTMS at all departments with active clinical trials.

Analyze the information submitted into the CTMS and the performance of the different services.
Keep track of the frequent asked question and answer all queries related to the implementation of the CTMS.
Keep up to date the eCRF and resolve queries in those clinical trial in which might be delegated
Collaborate and manage payments issues for those patients enrolled in clinical trials.
Give support in all activities entrusted by its manager.

Labour conditions: