Clinical Trial Manager Jobs in Tirol

1 - 6 von 6

Suchergebnisse - Clinical Trial Manager Jobs in Tirol

R&D Senior Quality Manager

Healthcare Businesswomen’s Association-Lienz

IT validations, etc. • Review and approve quality deliverables to ensure compliance (including procedures, records, third party work, contractors, clinical trial material, components, gap assessments ) • Reporting of technical complaints / adverse...

appcast.io - 1 Woche alt

6 ähnliche Jobs: Kufstein, Kitzbühel, Reutte, Imst, Innsbruck...

Expert Science and Technology in Analytical Operations

Novartis Pharma GmbH-Langkampfen

clinical trial and investigating the stability behavior of the drugs. Furthermore, we are validating the methods used for release and will be also responsible for transferring the methods to our commercial organization or external partners. The role...

myability.jobs - heute

Senior Expert - Analytical Operations (m/f/d)

Novartis Farmacéutica-Innsbruck

the product for clinical trial and investigating the stability behavior of the drugs. Furthermore, we are validating the methods used for release and will be also responsible for transferring the methods to our commercial organization or external...

appcast.io - 2 Wochen alt

6 ähnliche Jobs: Imst, Kufstein, Kitzbühel, Reutte, Landeck...

R&D Senior Quality Manager

Novartis Pharma GmbH-Langkampfen

inspection management • Support generation of Quality Plans (and review other plans for quality/safety aspects) for clinical programs • Support initiatives to maintain or improve quality performance and compliance of operational activities including...

myability.jobs - 1 Woche alt

Senior Expert - Analytical Operations (m/f/d)

Novartis Pharma GmbH-Langkampfen

Senior Expert - Analytical Operations (m/f/d) Summary About the role: #LI-Hybrid As a Senior Expert you will be part of a team developing new Biologic drugs. Analytical Operations is the team releasing the product for clinical trial...

myability.jobs - 1 Woche alt

RA CMC Postgraduate Intern

Novartis Pharma GmbH-Langkampfen

and strategic risks • Supporting and/or preparing high quality dossiers, drug substance and/or drug product quality documentation to support global regulatory submissions (e.g. Clinical Trial Applications, Market Authorization Applications, post-approval...

myability.jobs - 3 Wochen alt