Regulatory Affairs Jobs in Zug
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Suchergebnisse - Regulatory Affairs Jobs in Zug
Blueprint Medicines-Zug
to the International Regulatory Affairs Lead, the position will provide essential support in the planning and coordination of regulatory submissions as we continue for product launch(s) across our International business.
The individual will also ensure effective...
Acadia Pharmaceuticals GmbH-Zug
regulatory-related activities related to the launch of Acadia commercial products in each of the Member States of the EU and for ensuring the implementation of post-marketing requirements following marketing authorization. […]
Primary Responsibilities Leads...
job-room.ch -
Deciphera Pharmaceuticals, Inc-Zug
Senior Manager, International Medical Affairs
• Full-time
Deciphera, a member of ONO, is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. We...
GlaxoSmithKline-Zug
with regulatory authorities.
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
• Knowledge of pharmacology, physiology, clinical pharmacology, biopharmaceutics, regulatory affairs, therapeutics and commercialization...
appcast.io -
Flexsis-Zug
product development.
• Collaboration with internal stakeholders from R&D, production, quality assurance, regulatory affairs, project management.
• Familiar with software tools and databases for test management (Application Lifecycle Management tools...
GSK-Zug
Site Name:
USA
• Pennsylvania
• Upper Providence, Belgium-Rixensart, GSK HQ, USA
• Massachusetts
• Waltham, Zug House
Posted Date:
Dec 11 2024
Job Purpose
The Executive Director is accountable to the SVP, Regulatory Affairs Therapeutic Group...
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets.
Responsibilities
• Leads the pharmacovigilance agreement negotiation...
Regulatory Affairs Stellenangebote – Weitere Orte:
GlaxoSmithKline-Zug
career. These responsibilities include some of the following:
• Development and timely execution of practice changing Global Medical Affairs Plans (MAP) and Integrated Evidence plans (IEP) in partnership with key stakeholders through the GMAT and IET...
appcast.io -
GSK-Zug
with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries.
• Collaborate with Principal Investigators in the evaluation and assessment of publications (abstracts, posters, manuscripts...
Johnson & Johnson-Zug
development decisions, and labeling that support the commercial launch strategy in EMEA.
Leads the EMEA Integrated Brand Value Team, providing commercial strategic leadership and guidance into the brand regulatory strategy, medical affairs strategy...
Zug
development to demonstrate the value of Insmed’s products and support expediting patient access to Insmed’s medicines. The Senior Director, HEOR will work closely with Commercial, Market Access, Country Managers, and Global Medical Affairs teams to support...
icims.com -
GlaxoSmithKline-Zug
the following characteristics, it would be a plus:
Knowledge of pharmacology, physiology, clinical pharmacology, biopharmaceutics, regulatory affairs, therapeutics and commercialization such that he/she can assist in managing these interfaces and promote...
Deciphera Pharmaceuticals-Zug
Scientific Director and other functions.
• Provide tactical support to the medical affairs activities in the covered region.
• Act as scientific and medical review expert.
• Provide medical expertise in all regulatory, early access and reimbursement approval...
smartrecruiters.com -
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets.
Responsibilities
Leads the pharmacovigilance agreement negotiation...
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets
Responsibilities
Leads the pharmacovigilance agreement negotiation...
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