How do I apply for the Pharmacy Intern – Global Patient Safety (GPS) Department position at Ipsen and track my application?

We provide a direct link to the official application portal. You can apply directly here . Additionally, you can easily track this and other applications by clicking the bookmark icon to save it to your YGI Kanban board .

What are the working arrangements and expected duration for the Pharmacy Intern – Global Patient Safety (GPS) Department role?

This position is a full-time, structured as a on-site role, with an expected duration of 3 months.

What educational background or degree level is required for the Pharmacy Intern – Global Patient Safety (GPS) Department at Ipsen?

Candidates are generally expected to be holding or pursuing the following degree levels: Bachelor.

Does Ipsen provide visa sponsorship or assistance for international applicants?

Regarding visa assistance and sponsorship for this role, the official status is currently listed as: Not disclosed.

Pharmacy Intern – Global Patient Safety (GPS) Department

Ipsen

Found 2 months ago

Location

Paris, France

Duration (Months)

3 Months

Time

Full-time

Work Mode

On-site

Salary

Not disclosed

Visa Help

Not disclosed

Last Verified

2 months ago

Education

Bachelor

Skills & Qualifications

Technical Skills

pharmaceutical industry
drug development environment
adverse event management
signal detection
safety risk assessment
periodic safety reports
global pharmacovigilance processes
regulatory compliance

Soft Skills

Ability to adapt quickly and integrate into a team.
Autonomy and strong organizational skills.
Analytical and summarization capabilities.
Excellent interpersonal skills and ability to work in a multidisciplinary team.

Job Description

The pharmacy intern will support various activities within Ipsen’s GPS Department. Specific tasks will be assigned based on ongoing projects. This internship provides exposure to the key functions of a GPS department, including adverse event management, signal detection, safety risk assessment, and preparation of periodic safety reports. Through this experience, the intern will gain practical insights into global pharmacovigilance processes and regulatory compliance. The intern will also collaborate with cross-functional teams such as Regulatory Affairs, Medical Affairs, and Clinical Operations.

Requirements

Knowledge of the pharmaceutical industry and drug development environment.
Strong written and spoken English skills.
Ability to adapt quickly and integrate into a team.
Autonomy and strong organizational skills.
Analytical and summarization capabilities.
Excellent interpersonal skills and ability to work in a multidisciplinary team.

Medical, Clinical, and Veterinary

Physicians & Surgeons

Languages

English

Nice to Haves

Coordination with external ICSR (Individual Case Safety Report) service provider, ensuring the quality, accuracy, and clinical relevance of case safety reports.
Conduct a weekly review and quality check of Individual Case Safety Report (ICSR) listings to ensure accuracy and compliance.
Participation in the preparation of periodic safety reports (DSUR/PSUR) and Risk Management Plan (RMP) for marketed and investigational products.
Participation in signal detection, evaluation, and safety risk management activities.
Support for pharmacovigilance activities in clinical trials, including reviews of protocols and study reports.
Participation in cross-functional working groups and multidisciplinary project teams.
Attendance and contribution during GPS meetings.

Apply Now

8Open Positions