Clinical Trial Coordinator Assisted Reproduction

hace 7 meses

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

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 Coordinator**

**Assisted reproduction and gynaecological endocrinology Unit - Vall d'Hebron**

**Hospital**

The Obstetrics and Reproductive Medicine Department is a world leader in terms of the quality of its care, teaching and

research. For women who wish to become mothers and need technical assistance, we have a state-of-the-art assisted

reproduction laboratory. In addition, we care for pregnant women, considering the mother's health and that of the future

baby first and foremost, and always respecting the mother's wishes.

In the Assisted Reproduction and Endocrinology Unit we are developing a clinical trial to demonstrate the safety and

efficacy of a medical device that aims to improve the success of embryo transfers, and we are looking for a person with

project management experience to support the group of researchers involved in this study.***

**JOB DESCRIPTION**

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

University degree in the area of Life Sciences (e.g. Biomedical Sciences, Biotechnology, Biochemistry, etc.)
- Native level in Catalan and Spanish

**Desired: -**

English B2.1
- Project Management
- 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.**

**Experience and knowledge: -**

More than 10 years' experience in research laboratories, pharmacological laboratories and clinical analysis
laboratories.
- At least 5 years' experience in project budget management, purchasing, order tracking, inventory recording,
and stock control.
- Experience in information management, updating of databases, electronic passbooks or medical records.
- P experience in the use of highly complex laboratory equipment and biomolecule detection methods.
Experience in the handling of medical devices would be an asset.
- Knowledge of analytical procedures.
- Technical and communication skills.
- Ability to work in a team and to adapt, results-oriented and proactive.
- Knowledge of Good Clinical Practices, quality and safety regulations.

**Main responsibilities and duties: -**

Support investigators at different stages of the clinical trial to ensure that the clinical trial follows good clinical
practice.
- Responsible for identifying patients eligible for inclusion in the clinical trial.
- Responsible for the proper use and maintenance of the investigational medical device, as well as for the
recovery of the medical device and its consumable components once used.
- Responsible for the proper use, maintenance and updating of the clinical trial electronic notebook and for the
proper recording of source data in the investigator's folder.
- Coordinate with the VHIR Project Manager for the management of purchases of consumables, analytical tests,
etc.
- Coordinate with the Project Manager of the clinical trial sponsor to monitor the progress of the clinical trial
and/or possible incidents related to the investigational medicinal product, the electronic passbook, etc.
- VHIR-RRHH-FOR-003_v

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