GLOBAL PHARMACOVIGILANCE SR. SCIENTIST
Solo Talento
| (8) ofertas activas
Barcelona 19 Feb.
Somos una compañía de recursos humanos con más de 20 años de experiencia que ofrece Servicios de Consultoría de RRHH y de Selección de mandos intermedios, puestos técnicos y perfiles profesionales a nivel nacional e internacional.
Realizamos operaciones en numerosos sectores estratégicos de manera rápida y ágil gracias a la experiencia de nuestros consultores especializados.
Empresa que ofrece el puesto: Leading European specialty pharmaceutical companyRealizamos operaciones en numerosos sectores estratégicos de manera rápida y ágil gracias a la experiencia de nuestros consultores especializados.
Barcelona 19 Feb.
-
-
Descripción Leading European specialty pharmaceutical company focused on the treatment of the CNS built over 35 years is looking for a Global Pharmacovigilance Senior Scientist.
This company is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions.
This posicion is based in Barcelona, Sant Joan Despí (hybrid role)
You will report to the Corporate PV Manager
Responsibilities:
Support safety management activities of all the company’s products
Carry out PV activities in line with current local and global PV requirements and the company procedures
Monitor the adequate execution of activities delegated to our Global PV vendor
Review and make sure that PV contracts (national and international for the group) are up to date
Review of periodic safety reports and risk management plans prepared for our products worldwide
Monitoring and oversight of signal detection activities
Support the creation and implementation of risk minimisation measures, including PV educational materials for our products
Create standard operating procedures for the PV Department and propose improvements based on your experience
Ensure that PV activities for the company sponsored clinical trials are in line with company SOPs and applicable regulations
Participate in the preparation, execution and follow-up of PV audits and/or inspections
Support the setting up of the PV system for new countries and affiliates
Descripción Leading European specialty pharmaceutical company focused on the treatment of the CNS built over 35 years is looking for a Global Pharmacovigilance Senior Scientist.
This company is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions.
This posicion is based in Barcelona, Sant Joan Despí (hybrid role)
You will report to the Corporate PV Manager
Responsibilities:
Support safety management activities of all the company’s products
Carry out PV activities in line with current local and global PV requirements and the company procedures
Monitor the adequate execution of activities delegated to our Global PV vendor
Review and make sure that PV contracts (national and international for the group) are up to date
Review of periodic safety reports and risk management plans prepared for our products worldwide
Monitoring and oversight of signal detection activities
Support the creation and implementation of risk minimisation measures, including PV educational materials for our products
Create standard operating procedures for the PV Department and propose improvements based on your experience
Ensure that PV activities for the company sponsored clinical trials are in line with company SOPs and applicable regulations
Participate in the preparation, execution and follow-up of PV audits and/or inspections
Support the setting up of the PV system for new countries and affiliates
Número de vacantes:
1
Modalidad de trabajo:
Presencial
Tipo de contrato:
Indefinido
Requisitos
At least 5 years of experience within the pharmacovigilance disciplines in the pharmaceutical industry.
Experience in PV related environments, preferably at local, regional and global levels
Experience in Local/Global safety regulations and standards (e.g. ICH, EU Regulation)
Experience in Clinical Trial EU Regulation
Knowledge of legislation in force concerning pharmacovigilance.
Advance level management of MS word, MS excel, MS Access and MS Outlook.
Bachelor’s or master’s degree in life sciences (Degree in Pharmacy, Medicine, Biology, Chemistry or similar, Specific training in pharmacovigilance)
Fluent English and Spanish
Availability to travel: 10%
Experience in PV related environments, preferably at local, regional and global levels
Experience in Local/Global safety regulations and standards (e.g. ICH, EU Regulation)
Experience in Clinical Trial EU Regulation
Knowledge of legislation in force concerning pharmacovigilance.
Advance level management of MS word, MS excel, MS Access and MS Outlook.
Bachelor’s or master’s degree in life sciences (Degree in Pharmacy, Medicine, Biology, Chemistry or similar, Specific training in pharmacovigilance)
Fluent English and Spanish
Availability to travel: 10%
Estudios mínimos
Licenciado en Ciencias de la Salud
Especialidad: Degree in Pharmacy, Medicine, Biology, Chemistry..
Especialidad: Degree in Pharmacy, Medicine, Biology, Chemistry..
Idiomas
Inglés nivel Alto.
Experiencia mínima
5 años
Disponibilidad para viajar
El 20% del tiempo laboral