In this role, you will support key functions in the clinical research area as part of the Submission Delivery Excellence team.
This is a great opportunity to gain knowledge of preparing and delivering documentation in clinical research projects. You will learn how to ensure documents are compliant with regulatory standards, internal GSK processes and policies, as well as timeliness.
This role mirrors the tasks of a CTA/IND Registration Specialist in a multinational pharmaceutical company.
We encourage you to apply :)
what we offer- opportunity to participate in training and improve skills
- opportunities for development within the company structure
- flexible hours of the internship
- contract of mandate
- hourly rate of PLN 34 gross/hour for the first 6 months, with the possibility of extending the internship to 12 or 18 months, the rate for the next period of PLN 37 gross/hour
- Randstad Plus - a system of benefits (sports card, private medical care, discounts for online shopping)
- possibility of breaks in the internship due to vacation plans
- possibility of employment by GSK after completing the internship
- support in coordinating Clinical Trial Authorization (CTA) submissions and ensuring compliance with regulatory requirements and GSK policies
- archiving and organizing regulatory documentation
- participating in the maintenance of regulatory information management systems and trackers (e.g., post-approval activity data)
- university degree in pharmacy, chemistry, biological sciences, health sciences or other related field
- interest in regulatory affairs (Regulatory Affairs), clinical trials and pharmaceutical industry
- good oral and written English skills (B2+/C1)
- ability to solve problems, organize work and manage time
- minimum availability: 25h/week (30-35h/week preferred)
Employment agency entry number 47
this job offer is intended for people over 18 years of age
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