17.09.24 | Vollzeit | Baar | JobLeads GmbH | CHF 125’000 - CHF 150’000 Education and enquiry management from investigators and staff engaged in GSK-supported clinical trials. - Fully understand and comply with GSK standards and policies and with local codes of practice, guidelines and laws to ensure the strictest requirements are met. Basic Qualifications - Degree in life
Später ansehen10.09.24 | Vollzeit | Baar | JobLeads GmbH | CHF 125’000 - CHF 150’000 Promotional materials, management monitoring, risk management and handling of Article 71 requests. 2. Act as Named Safety Contact for Switzerland with overall responsibility for the day-to-day management of pharmacovigilance activities for marketed products and products in clinical trials, including all
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
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