15.09.24 | Vollzeit | Zug | JobLeads GmbH | CHF 125’000 - CHF 150’000 As well as with company policies. You will develop and implement strategies for timely submissions and approvals of pre-clinical submissions, applications for clinical trials, and marketing applications. Providing counsel to your Regulatory Affairs team, your expertise in both indirect and direct markets
Später ansehen01.09.24 | Vollzeit | Zug | JobLeads GmbH | CHF 80’000 - CHF 100’000 In international markets. - Ensure CMC part of the regulatory submissions meets ICH and regional/local regulatory requirements. - Perform CMC regulatory submissions including clinical trial applications, amendments, supplements thereof, marketing authorizations, post-approval variations, periodic reports
Später ansehen30.08.24 | Vollzeit | Zug | JobLeads GmbH | CHF 80’000 - CHF 100’000 Perform CMC regulatory submissions including clinical trial applications, amendments, supplements thereof, marketing authorizations, post-approval variations, periodic reports, and license renewals. - Ensure timely discussion, and negotiation as necessary, with local/international health authorities
Später ansehen06.11.19 | Vollzeit | Zug | headcount AGIncluding publications and clinical trial databases, and produce reports on the medical background, treatment guidelines, drug mode of action, and competitive product
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