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Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!
Job Responsibility:
To perform systematic literature search for regulatory or scientific documents
To assist managers in the preparation of pre-clinical or clinical sections of the marketing authorization dossier
To assist the manager and preparation of various toxicology assessments like PDE/OEL or other toxicology documents
To assist managers in preparation of other medical-scientific documents (e.g., publications, product rationales, medico-marketing material)
The employee agrees to take over additional reasonable tasks that align with their abilities, if required
Requirements:
Autonomous, concentrated and high-quality work
Ability to work in a team
Sense of responsibility
Basic knowledge of marketing authorization procedures in the EU
Basic knowledge of economic principles
Very good command of English
Strong communication and interpersonal skills
Excellent in MS Office package and well-versed with various literature