Pharmacovigilance Internship — Med Safety in Madrid

Johnson & Johnson Co.; Madrid; On-site; EUR 10,000 - 15,000; Full time

Benefits offered by this job

1 year internship

Full-time internship

Madrid location

Job summary

Johnson & Johnson is seeking a Pharmacovigilance Trainee for a 1-year internship in Madrid. The role reports to the Country Safety Head and supports Safety and Risk-Benefit activities at the Local Operating Company level.

Responsibilities include collecting and processing adverse events, follow-ups, translation of documents, ICSR submission oversight, literature searches, and maintaining archives per retention schedules.

Qualifications

• Education: Pharmacy or Life Sciences.
• Fluency in local language(s) and in English is required.
• Strong organizational skills, attention to detail and accuracy.
• Creativity, thinking outside of the box.
• Acquires knowledge of PV Procedural Documents.

Responsibilities

• The Pharmacovigilance Trainee provides support to the Country Safety Head, LSO back-up and Local Medical Safety Specialist in all administrative aspects of Safety and Risk-Benefit Management and Reporting at the Local Operating Company level.
• Collection, triage, evaluation and processing of all AEs, AE/PQC and SS (ICSR) within the Global Safety System from various sources.
• Follow-ups for missing information and/or requests by GMS.
• Translation of source documents, including EudraVigilance downloads.
• Reconciliation activities and oversight of ICSR submission to regulatory authorities.
• Literature search and related activities; local archive management and document retention.

Skills

Fluency in local language(s)

Fluency in English

Education

Pharmacy or Life Sciences

Job description

Johnson & Johnson is seeking a Pharmacovigilance Trainee for a 1-year internship in Madrid. The role reports to the Country Safety Head and supports Safety and Risk-Benefit activities at the Local Operating Company level.

Responsibilities include collecting and processing adverse events, follow-ups, translation of documents, ICSR submission oversight, literature searches, and maintaining archives per retention schedules.