Medical Affairs Expert

Für unseren Kunden, einen führenden Anbieter von medizinischen Geräten und pharmazeutischen Produkten in der Zentralschweiz, suchen wir eine engagierte Persönlichkeit alsMedical Scientific Affairs Manager (w/m/d)Ihre Aufgaben- Fachlicher Support zu medizinisch wissenschaftlichen Produktaussagen in den Bereichen Haut- und Wundmanagement- Planung und...

Für unseren Kunden, einen führenden Anbieter von medizinischen Geräten und pharmazeutischen Produkten in der Zentralschweiz, suchen wir eine engagierte Persönlichkeit alsMedical Scientific Affairs Manager (w/m/d)Ihre Aufgaben- Fachlicher Support zu medizinisch wissenschaftlichen Produktaussagen in den Bereichen Haut- und Wundmanagement- Planung und...

Job DescriptionAs a (Associate) Principal within the Medical Evidence Practice (MEP) team, you will take on a variety of roles within the following core areas: business development, client relationship building, project leadership, and team development.The role requires an inquisitive, consulting mindset to develop new opportunities, alongside a...

Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche,...

The Position Internship Purpose:  This 12-month internship offers an opportunity to gain hands-on experience of global medical affairs activities at an innovative and patient-centric global pharmaceutical company. You will be working on a project in the Ophthalmology or Nephrology disease area that aims at fostering scientific exchange between Roche...

At Novartis Farmacéutica, we are seeking a Medical Safety Expert to join our Oncology Medical Safety organization. This role is part of our Radioligand Therapy team and offers the opportunity to make a significant impact on patients' lives.About this Role:The Global Program Lead - Oncology will excel as a scientific safety leader, providing expert safety...

As an integral part of the Global Medical Affairs team, you will play a key role in implementing the Medical Information strategy. You will drive its execution by delivering high-quality content, reports, and product-specific support to both internal and external stakeholders.Responsibilities:Ensuring an effective and audit-ready Global Medical Information...

Global Regulatory Affairs Strategist (New Product Developments)About Us: North Star is a rapidly expanding consumer healthcare business with a strong European presence. We are committed to delivering high-quality products/services and exceptional value to our customers. We are seeking a highly skilled and motivated Regulatory Affairs Strategist to join our...

Roche's Clinical Development organization is responsible for developing and executing the clinical development strategies and plans that deliver medically differentiated therapies. The Principal Medical Director will focus on guiding the development of our MS & Neuroimmunology portfolio.The ideal candidate will have extensive experience in Neuroimmunology...

Join Roche's Clinical Development organization as a Principal Medical Director and contribute to the development of our MS & Neuroimmunology portfolio.As a member of our team, you will lead Clinical Development (CD) strategy and ensure effective execution for assigned molecules/indications.This position requires a strong understanding of Neuroimmunological...

About the Position:The Global Program Safety Lead is responsible for managing safety issues from the formation of the Global Program Team through Life Cycle Management. This involves providing expert safety input to clinical development programs for assigned projects/products, actively participating in the Global Program Team, Global Clinical Team, and...

We are seeking a highly skilled and experienced Medical Information Specialist to join our team at Skilled Recruitment Solutions GmbH.About the Role:This is an exciting opportunity to play a key role in implementing the Medical Information strategy, driving its execution by delivering high-quality content, reports, and product-specific support to both...

Skilled Recruitment Solutions GmbH is committed to excellence in Medical Information management. We are seeking a seasoned Global Medical Content Manager to join our team and drive the implementation of our Medical Information strategy.About the Job:This key position involves delivering high-quality content, reports, and product-specific support to internal...

Job Overview:">Skilled Recruitment Solutions GmbH is seeking a Clinical Scientist to support the development of clinical trials within the pharmaceutical industry.">This role requires a strong background in clinical research, with experience in protocol development, data review, and medical monitoring.">The successful candidate will work closely with...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.Abbott...

RequirementsTo succeed as a Regulatory Affairs Support Professional, you must have relevant Swiss working/residency permit and/or Swiss/EU citizenship.Candidates should have expert user experience in SAP MM and PP, and good knowledge of business systems and tools.A strong focus on excellent communication skills and attention to detail is essential for this...

Job Description:The PositionWe are seeking an experienced Principal Medical Director to join our Neuroimmunology Team within the Neurology Therapeutic Area. The successful candidate will be responsible for guiding the development of our MS & Neuroimmunology portfolio.Key Responsibilities:Lead Clinical Development (CD) strategy and ensure effective execution...

Regulatory Affairs LeadWe are seeking a highly motivated Regulatory Affairs Lead to join our team. The successful candidate will be responsible for ensuring compliance with GMP regulations.Main Responsibilities:Conduct thorough reviews and approvals of analytical methods, method validations, specifications, risk assessments, deviation reports,...

Lonza Biologics Porriño SLU is a global leader in life sciences operating across three continents. We work in science, but our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.The role of Director, Local Lead Regulatory Affairs Advanced Synthesis within our Advanced Synthesis Platform...

About the Role: We are seeking a highly skilled Regulatory Affairs Strategist to join our dynamic team and drive the regulatory strategy for new product developments.We offer a collaborative and inclusive work environment where you can grow your career and contribute to the success of our organization. As a member of our team, you will be responsible for...