TRIUM Clinical Consulting NV seeks an Associate Consultant to join the Regulatory Affairs & Publishing team on a hybrid basis in the UK. The role targets early-career professionals eager to develop in regulatory submissions and dossier publishing for pharma, biotech and medical devices.
You will start with day-to-day activities, gradually taking on more responsibility, while benefiting from mentoring and a collaborative team across life sciences.
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Contact Details:
TRIUM Clinical Consulting NV Recruitment Team
