In mcr international we are collaborating with a multinational pharmaceutical company that is looking for a pharmacovigilance & medical information specialist to join the barcelona team.
departament: regulatory affairs, quality assurance and pharmacovigilance.
reporting to: regulatory affairs, quality assurance and pharmacovigilance manager.
mission:
ensures that the company has systems and processes to collect, record, report and follow up on suspected adverse reactions.
responsible for liaising with the competent authorities on pharmacovigilance matters and representing the company in dealings with these authorities.
responsible for answering product inquiries; include questions about drug information or adverse reactions.
número de vacantes: 1
modalidad de trabajo: presencial
tipo de contrato: indefinido
"
*requisitos*
*responsibilities*:
be the local contact for pv (e.g., for inspections, recalls, urgent safety restrictions, etc.)
receive and handle medical information enquiries from patients and health care professionals
first line of defence against potential safety issues
report adverse events and carrying out risk management activities help keep patients safe and ensure that medicines remain effective
comply with local, regional, and global pv legislation
implement, oversee, and ensure functioning of the local pv system
perform pv training of employees
support the eu qppv
review of promotional and non-promotional materials
*requirements*:
academic degree in life science and pharmacovigilance..
2 years' experience with local pharmacovigilance activities.
fluent in english, fluent italian language skills would be additional benefit.
strong organizational and time management skills.
active listening and effective communication.
ability to work independently and in a team.
en ciencias de la salud
estudios mínimos
licenciado
*idiomas*:
inglés nível alto.
experiência mínima
2 años
disponibilidad para viajar
ninguna