FAQs
What is the duration of the Pharmacovigilance Intern position?
The Pharmacovigilance Intern position is for a duration of 12 months.
Who will the intern report to during their internship?
The intern will report to the RA/aPV Country Lead.
What type of experience will the intern gain in this role?
The intern will gain hands-on experience in the pharmaceutical industry, working closely with a mentor in a dynamic, multidisciplinary environment.
What are the key responsibilities of the Pharmacovigilance Intern?
Key responsibilities include managing adverse event cases, participating in PV activities like case processing and audits, completing training courses, and supporting local PV audits and inspections.
What qualifications are required for this internship?
Required qualifications include post-graduate education in pharmacovigilance or a related field, a degree in health, life science, or medical science, and fluency in English.
Is proficiency in any language other than English beneficial for this position?
Yes, proficiency in French is considered a plus.
What competencies and skills are expected from the intern?
Interns should have good time management, organizational, and collaboration skills, strong communication skills, and a basic understanding of regulations and compliance related to pharmacovigilance.
Will the intern be involved in compliance-related tasks?
Yes, the intern will be involved in ensuring compliance with global and local regulations and supporting audits and inspections related to pharmacovigilance.
Are there training opportunities within this internship?
Yes, the intern will complete company training courses and stay updated on local and EU legislation.
What technical skills are required for this internship?
Interns should be proficient in word processing, presentations, spreadsheets, and have the ability to learn new systems quickly.