Biogen Jobs in Schweiz

As an apprentice Chemical and Pharmaceutical Technologist you will play a key role in supporting the full manufacturing process of our medicines from initial raw materials to concentration and filling. · ...

The EU CTR Submission Specialist is responsible for planning and managing regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). · This role covers the entire lifecycle of a ...

The International Commercial Lead will be the cross-functional leader of the SMA International Center of Excellence, · leading the cross-functional integrated customer strategy and navigating the international organization through the Spinraza High Dose launch, · defining competi ...

+p>Job summary+/The International Commercial Lead will be the cross-functional leader of the SMA International Center of Excellence.+/p> · +/h2>Responsibilities+/ · +ul>Lead the cross-functional partners (Marketing, Medical, Market access, Patient Advocacy Groups /communications, ...

The EU CTR Submission Lead is responsible for leading and overseeing the full lifecycle of regulatory submissions for clinical trials conducted under the EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). · This role provides strate ...

The EU-CTR Submissions Group Lead is a critical leadership role overseeing operational activities related to end-to-end trial submissions and lifecycle management under the EU Clinical Trials Regulation (EU CTR 536/2014). The position ensures the efficient, timely, and compliant ...

+ Lead regional Regulatory Affairs activities for biosimilars beyond centralized authorizations. · + Oversee product updates across multiple countries and manage key national regulatory process steps. · + Build strong relationships with affiliate and distributor teams to support ...

A Sr. Logistics Specialist will be a vital member of our International Logistics & Customer Service team, ensuring smooth distribution and logistics operations. · ...

This role plays a pivotal part in shaping and executing the global Regulatory Chemistry Manufacturing and Controls strategy for Biogen's small molecule portfolio.You will be responsible for leading cross-functional regulatory CMC activities to ensure timely preparation and delive ...

The International Marketing Lead is accountable for all ex-North America marketing deliverables for SPINRAZA.To enable continued growth of the brand, they will coach the SMA Marketing team in refining near-term Marketing strategy and short-term execution. · The incumbent will wor ...

As a Sr. Logistics Specialist,you'll be a vital member of our International Logistics & Customer Service team, · You will manage complex international shipments and the operational delivery of the order-to-cash process for diverse distribution models. · Supervise and manage opera ...

+p>Job summary · The Global Medical Affairs Director, Epilepsy will be a strategic partner providing expert medical leadership to guide development, launch planning, and support for zorevunersen to improve meaningful patient outcomes. · +Responsibilities · Develop and implement t ...

The EU CTR Submission Specialist is responsible for planning, preparing, managing, and maintaining regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role covers the ...

As the Global Commercialization Lead you will be responsible for delivering the Disease Area Strategic Plan (DASP), working closely with regions to execute and evolve the global commercialization strategy. · ...

As Manager Regulatory Affairs you will lead regional RA activities for biosimilars beyond centralized authorizations coordinating with Affiliate RA to identify and fulfill national regulatory requirements to support successful product launches. · ...

As the Associate Scientific Director, Clinical Pharmacology you will serve as the clinical pharmacology lead on program and study teams providing strategic leadership in the development and execution of clinical pharmacology plans for drug candidates. · ...

The Global Commercialization Lead will be responsible for delivering the Disease Area Strategic Plan (DASP), working closely with regions to execute and evolve the global commercialization strategy. The role will report to the Product Development and Commercialization Lead (PDC), ...

The EU CTR Submission Specialist is responsible for planning and managing regulatory submissions for clinical trials in compliance with the EU Clinical Trial Regulation via the Clinical Trials Information System. · ...

+ As Manager, Regulatory Affairs you will lead regional RA activities for biosimilars beyond centralized authorizations coordinating with Affiliate RA to identify and fulfill national regulatory requirements to support successful product launches.+ You are a motivated and quick l ...

The International Marketing Le a d is accountable for all ex-North America marketing deliverables for SPINRAZA. · ...