17.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 Timelines. Partnering with industry leaders, we aim to transform drug development with unparalleled efficiency and flexibility. Our team leads key industry standardization initiatives and combines extensive experience in platform based drug development innovation & research acceleration. Over the past year
Später ansehen16.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 200’000 - CHF 250’000 Evidence plans and study designs in collaboration with cross-functional teams. - Provide medical input into study designs, evaluate scientific protocols, and oversee study execution. - Build partnerships with key scientific and medical opinion leaders to support health initiatives. Requirements - MD
Später ansehen17.06.24 | Vollzeit, Freelancer | Berlin | Hays AG - internNext -> Kontakt Mein Hays Menü Zum Hauptmenü Zurück Mein Hays @ @ @ @ @ @ - = = = - = = - @ @ @ - = - = = = - @ @ o @ @ @ @ - @ o @ @ @ - = = - = = = = = = = = - = = = = - @ - @ - @ o @ @ @ o @ @ @ @ - = = = = = = = - @ @ - o @ - = = = = = = = - = = = = = - @ @ @ @ - @ - @ @ - = = - @ @ MEINE MERKL
Später ansehen16.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 Assist in authoring key clinical study documents, including Protocols, Clinical Study Reports, Investigator Brochures, Regulatory Authority briefing books, Development Safety Update Reports etc. - Responsible for medical monitoring of efficacy and safety clinical trial data. - Strategic input
Später ansehen17.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 And executing them. Your key responsibilities, but not limited to; - Lead the team responsible for the Aggregate Reports & Risk Management office, the quality standards and metrics and the strategy team. - Enable the tools that support transversally all sub functions in the department. These include
Später ansehen14.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 Assist in authoring key clinical study documents, including Protocols, Clinical Study Reports, Investigator Brochures, Regulatory Authority briefing books, Development Safety Update Reports etc. - Responsible for medical monitoring of efficacy and safety clinical trial data. - Strategic input
Später ansehen16.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 With Business Partners. Job Description Your Key Responsibilities Your responsibilities include, but not limited to - Partner with P&O colleagues and other business stakeholders to create, update and review existing and new P&O processes, documents (policies/guidelines/templates etc.) in relation to Sandoz
Später ansehen18.05.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 And financial community, hosting important meetings and engaging with key stakeholders. You will also represent the Bank at key international forums such as the G20. This is an exceptional opportunity to contribute to the pursuit of monetary and financial stability through international cooperation. You
Später ansehen12.06.24 | Vollzeit | Basel (Basel-Stadt) | Randstad Schweiz AGA leading pharmaceutical company is looking for a PMO Audit Coordinator. This role is based in Basel, Switzerland. Background As SME of the Risk & Audit Framework, you will play a key role in the related contribution to achieve a higher maturity in the area of governance, risk management
Später ansehen17.06.24 | Vollzeit, Trainee | Murten | jobwinner.chMedical communication, key opinion leader management, clinical initiatives, medical marketing, and sales and marketing support. - You are a hands-on person who knows how to
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