Internship: Pharmacovigilance Intern

3 settimane fa


Siena, Toscana, Italia GSK A tempo pieno
工作地點名稱: Italy - Siena
刊登日期: May

Posting Title: Internship: Pharmacovigilance Intern (SERM) Italy - 2024

Help us get ahead of disease together with our Safety Eval, & Risk Management Italy Team

Education required:

  • Master's Degree in scientific field (Pharmacy/CTF, Biology, Chemistry, etc.)
  • II Level Master in Pharmacovigilance or similar (Preferred)

.

Other requirements:

  • Good communication skills
  • Team spirit
  • Agility and attitude of problem-solving
  • Strong work ethics
  • Good spoken and written English

Application deadline: April 11th

Duration: 6 Months

Start date: May 2024

Type: Curricular or Extra-Curricular Internship

100% presence

Looking to gain valuable real world work experience and help positively impact the health of billions of people? Apply for a GSK Internship today

A GSK internship offers you the opportunity to kickstart your career – to take on a real role with genuine impact You'll take on challenging, serious work on live projects or assignments. You'll also get to learn from us, develop your skills and gain valuable experience for wherever the future takes you.

What will you do?

The Intern will operate within the Department of Safety Evaluation & Risk Management (SERM) in the Siena (Italy) Research & Development site. The department is part of the Vaccines Safety Department within Global Safety at GSK. The Intern will support the work of the safety specialists responsible for the clinical safety and pharmacovigilance of vaccines.

Project description

The main purpose is to train the Intern to gain experience in a wide range of clinical trial safety and pharmacovigilance activities. These activities are reaching from literature review to safety signal evaluation in clinical trials and post-marketing safety of licensed vaccines. The Intern will support the preparation of aggregated periodic reports for submission to Regulatory Authorities.

Competencies the intern will develop thanks to the internship experience

The candidate will gain a good understanding of the clinical trial safety and pharmacovigilance processes in the global pharmaceutical setting, and detailed knowledge of the GVP regulations.

Let's do this

You'll find hints, tips and guidance on our recruitment process on our website –

Learn more about the application process | GSK

We recommend you apply as soon as possible, because we accept ongoing applications and offer positions on a first come, first served basis.

Apply now

Need help with your application?

Please email us at and let us know how we can help you.

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