LF-2502-90
PHARMACOVIGILANCE & MEDICAL INFORMATION SPECIALIST
BARCELONA

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.

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.

Detalles / Details