Medical Studies Coordinator

2 days ago


Stockholm, Stockholm, Sweden PharmaRelations ApS Full time
About the Role:

We are seeking a Clinical Affairs Specialist to join our team to work on the design and coordination of CC sponsored clinical studies for new and currently licensed products to support marketing approval of products and functions.

This role requires close collaboration with the Critical Care business area and other stakeholders to ensure timely completion of studies and compliance with regulatory requirements. The ideal candidate will have a strong understanding of Good Clinical Practice, ISO 14155, and experience within the Medical Device industry and/or the life science industry.

You will be responsible for managing and executing post-market clinical research studies and surveys, ensuring compliance with legal and regulatory requirements, and monitoring audit readiness of clinical study data and documents at sites.



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