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Paid Internship
Work Mode
Time Spent
Required Degree
Duration

12Open Positions

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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.

Related Field

  • Medical, Clinical, and Veterinary

Related Subfield

  • 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

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