Clinical Trial Supply Manager managing packaging and labelling of investigational products for clinical studies. Working in a team-oriented environment and ensuring regulatory compliance.
Responsibilities
Act as a CTS specialist in Orion’s clinical studies.
Preparing label texts for investigational products.
Designing and preparing clinical study labels.
Planning and coordinating the packaging and labelling of investigational products.
Participate in packaging and labelling work when needed.
Inspecting packaging and labelling work and documents.
Organising the distribution of investigational products to clinical study sites.
Documenting, reviewing and approving different CTS documents.
Participate in the development of our operations.
Participating in the evaluation of service providers and participating e.g. preparation of requests for proposals and QA-agreements.
Acting as a contact person.
Monitoring the work performed and reviewing and approving the required documents.
Requirements
MSc degree in Pharmacy.
To be precise and eager to take on new tasks.
Good organizational skills, and the ability to manage your workload effectively, even when handling multiple tasks simultaneously.
Strong teamwork skills.
Proficiency in both spoken and written Finnish and English.
Benefits
An interesting, challenging role that includes also hands-on work and outsourcing.
A nice working atmosphere based on a good team spirit and friendly colleagues.
A comprehensive training for your tasks, and thereafter, our senior-level experts in our CTS-team will support you in carrying out your tasks.
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