The Clinical Research and Clinical Trials Area of INCLIVA works to promote and facilitate the conduct of studies that contribute to the advancement of medical knowledge and to the improvement of healthcare. We support both the comprehensive management of independent clinical studies and the clinical trials sponsored by the pharmaceutical and medical device industry.

To this end, the area offers advice and support in all phases of study development, ensuring compliance with current regulations, good clinical practices, and the highest quality standards. In this way, INCLIVA reinforces its commitment to clinical research as a driver of innovation and of the transfer of results to clinical practice.

Functions:

  • Processing of the suitability of the facilities.
  • Management of contracts between the sponsor and the site.
  • Negotiation of the financial reports.
  • Billing of clinical trials (CTs).
  • Monitoring services.
  • Project management services.
Contact

General information:
investigacionclinica@incliva.es

Management of the Suitability of the Facilities:
ensayosclinicos@incliva.es

Contracts and Financial Reports Management:
contratoseecc@incliva.es

Billing:
facturacioneecc@incliva.es

Clinical Research and Clinical Trials Unit (UICEC):
uicec@incliva.es

Management of the Suitability of the Facilities
Contracts and Financial Reports Management
Billing
UICEC
Clinical Research Units
Phase I Oncological Clinical Trials Unit

Team

Administrative assistant

Manuela Erasun

Contract Management

Miguel Roig

Economic management
.

Mayca Román

Clinical trials management

Sofía Galant

Clinical trials management

Sara Jordá

Clinical trials management

Miriam Stumpf

Clinical trials management

Jacobo Bolinches

Clinical trials management

Marta Martínez

Clinical trials monitoring

Ana Portolés

Clinical trials monitoring

Mercedes Peris