Project management of the preclinical development of medicinal products including the writing of regulatory documents
As a Junior Project Manager you will use your scientific expertise to assist with multiple projects which will include planning and managing preclinical development (pharmacology, toxicology, manufacture) together with writing regulatory documents.
Key duties and responsibilities:
The duties will be varied but will principally comprise:
Whilst training will be given, knowledge or experience of the preclinical development of medicinal products will be viewed favourably. International experience as well as some industrial training will also be considered advantageous.
This will be a permanent position with opportunities for growth and promotion, based in Paris (France), with a competitive salary, together with a bonus scheme awarding outstanding performance.
The recruitment process will be initiated with a short informal virtual meeting to discuss the candidate’s background and motivation. This is followed by a more formal interview with the two company directors which may be in-person or virtual depending on the candidate’s circumstances. The final stage is a presentation to the senior team as well as the opportunity to informally chat with team members.
Please note that applications must be in English and unfortunately applications in French will not be considered, as this position requires a very high level of written and spoken English.
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