CRA II: Gynecologic Oncology Trials, Barcelona

Fortrea; Barcelona; Presencial; EUR 42.000 - 56.000; Jornada completa

Descripción de la vacante

Fortrea in Barcelona is seeking two CRA2 professionals to join our FSP team to monitor complex clinical trials in Gynecologic Oncology or Onco-Hematology. The role includes site monitoring, ensuring patient safety, data integrity, and adherence to regulatory requirements.

Will liaise with vendors, coordinate visits, and support regulatory submissions. Travel may be required, and fluency in Spanish and English is essential.

Formación

• University Degree in Scientific/Medical Field is required.
• Strict adherence to ICH GCP guidelines and local regulations.
• Fluency in Spanish and English (written and spoken).

Responsabilidades

• Monitor study sites for complex trials in Gynecologic Oncology or Onco-Hematology.
• Ensure informed consent processes and protocol requirements are followed.
• Maintain source data integrity and perform CRF review.
• Collaborate with vendors and internal teams to manage timelines and resources.
• Facilitate site initiation visits, monitoring visits, and closeout activities.
• Travel as required, prepare trip reports and document regulatory submissions.

Conocimientos

Site monitoring

ICH GCP knowledge

Bilingual Spanish/English

Educación

University Degree in Scientific / Medical Field

Descripción del empleo

Fortrea in Barcelona is seeking two CRA2 professionals to join our FSP team to monitor complex clinical trials in Gynecologic Oncology or Onco-Hematology. The role includes site monitoring, ensuring patient safety, data integrity, and adherence to regulatory requirements.

Will liaise with vendors, coordinate visits, and support regulatory submissions. Travel may be required, and fluency in Spanish and English is essential.