Stellenangebote für Drug Regulatory Affairs Manager Jobs in der Schweiz

20 Treffer

Sr. Regulatory Affairs Project Lead Pharma

Top Job - Baden

Innovative products is needed. As a Senior RA Manager you are responsible for proactive and efficient management of all regulatory aspects for the assigned product and assume a cross-functional leadership role for the NDA and MAA...

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Junior International Drug Regulatory Affairs Project

Top Job - Bern, Genève, Basel (Basel-Stadt), Zürich

Details Hays Blog Social Media Kontakt Suche Land wählen Deutsch English Fran ais DE EN FR Land wählen Australien Belgien Brasilien Chile China Dänemark Deutschland Frankreich Grossbritannien u. Nordirland Hongkong Irlan...

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Clinical Program Data Manager

Top Job - Zug

A contact representing DM within Biometrics and clinical study management teams (SMT and/or Clinical Development Team representatives). Liaises directly with internal customers (Biometrics functions, GCO, Regulatory...

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Clinical Trial Associate - 2 years fixed term contract

- Boudry

Departments such as, Investigational Medical Product Supply Chain (IMSC), RegulatoryAffairs, etc. - Maintain and track documents such as Investigator Brochures (IBs), insurance policies, documents that are expiring and IND safety...

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DRA Coordinator

- Rotkreuz

Approval of printed packaging material sheet (PPMS). " Ensures optimal launch preparations for new products in close collaboration with the regulatoryaffairsmanager (RAM), product management, local and global supply chain...

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Project Director

- Premier

Ensuring successful management and coordination of efforts assigned to members of the global project team, including Regulatory, Clinical Operations, Biometrics, and Medical Affairs/Safety, to support milestone achievement and...

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Clinical Development Medical Director Oncology

- Basel (Basel-Stadt)

Deliverables may include clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration...

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Clinical Development Medical Director - Oncology

- Basel (Basel-Stadt)

May include clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration...

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Senior Business Systems Analyst ? EDMS

- Basel (Basel-Stadt)

regulatoryaffairs Experience in development of training documentation and eLearning Modules and providing end user training Strong knowledge in system management and administration Strong knowledge of Computer System Validation...

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Clinical Development Medical Director - Anti-Infectives

- Basel (Basel-Stadt)

Deliverables may include clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration...

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Senior Manager, Regulatory Projects Team

- Boudry

Are developed in alignment with Global RegulatoryAffairs (GRA) and the Global Project Team (GPT) · Maintains awareness of emerging issues that may impact regulatory product strategy and Celgene EU regional business...

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Clinical Development Medical Director Anti Infectives

- Basel (Basel-Stadt)

218405BR Position Title Clinical Development Medical Director Anti Infectives Division Global Drug Development Business Unit CD&A GDD Country Switzerland Work Location Basel Company/Legal Entity Novartis Pharma AG Functional...

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Regulatory Program Manager EU

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Colleagues from DrugRegulatoryAffairs (DRA) Affiliates, Pharma Technical Regulatory (PTR), Diagnostics Regulatory and in PD across the product life cycle to deliver high quality medicines. In this role youll be responsible...

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DRA Coordinator

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Job ID 223992BR Position Title DRA Coordinator > Development Business Unit REG AFFAIRS GDD Country Switzerland Work Location Rotkreuz Company/Legal Entity Novartis Pharma Schweiz AG Functional...

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Medical Science Liaison (Austria& Switzerland)- Rare

Top Job - Cambridge, Zug

Least experience in rare diseases - Working knowledge of RegulatoryAffairs, Drug Safety, Legal and compliance environment. - Matrix management experience with the Regional Offices and...

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