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The Director Clinical Affairs plans, implements and manages clinical trials and influences study design and interprets results. She/He defines clinical trial protocols, standard...
This role is responsible for the implementation of global CMC regulatory strategies specific to Viatris’s Biologics and biosimilars products. Working in partnership with key...
Accountable for all activities of site related study execution of assigned studies/Monitors involving start-up, execution, and close-out. Accountable for the on-time and within...
Alnylam seeks a highly motivated Senior Manager, Regulatory Affairs, to manage the European regulatory activities of products in late stage development through to gaining marketing...
Manages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. Develops clinical tools (e.g. Monitoring Plan,...
This position is responsible for providing audit support and GCP oversight of Clinical Development teams to the Head of Incyte Global R&D QA GCP/PhV. This job will include the...
In this leadership role, you will be directly responsible for the management of the Clinical Project Leaders, Site Partnership Managers, the Clinical Trial Application Regulatory...