Regulatory Affairs - Industrial Placement Review
at Vertex Pharmaceuticals
Placement (10 Months+)
Medicine
London
Review Submitted: July 2022
Overall Rating
3.8 /5
The Overall Rating is the average of all the ratings given in each category. We take those individual ratings and combine them into one final score!
Overview of Role
Please give an overview of your role and what this involves on a day-to-day basis.
- Preparation of documents to send to regulatory health authorities.
- Compiling correspondence and submission content to create trackers for multiple clinical trial studies.
- Archiving regulatory correspondence in Veeva Vault RIM for study tracking progress.
Were you given much responsibility during your placement / internship?
Please rate how meaningful the work you were doing was
Skills Development
Have you learnt any new skills, or developed your existing skills?
- Understanding of the drug development, regulatory landscape and clinical trial process.
- Improved communication and time management skills