Roles & responsabilities:
-
Responsible for the processing of safety information from both postmarketing and clinical trials ensuring compliance towards regulatory requirements and internal SOP.
-
Operational support to Clinical trial activities (SAE management, reconciliation, unblinding activities and safety monitoring activities during development).
-
Support in PSUR preparation, signal detection activities, literature reviews and archiving.
-
Responsible for electronic transmission related activities.
-
Create, update and review of SOPs and WI related to safety operational activities.
Prerequisites:
-
Health Sciences Degree.
-
2-3 years experience in pharmacovigilance.
-
Good knowledge of medical terminology.
-
Fluent in English.
Empresa:
RPS Research Ibérica S.L.U.
Persona de Contacto:
Cristina Jiménez
Ciudad: Barcelona.
Dirección: Via Augusta 21-23, Planta 5ª
Código postal: 08006
