Clinical Scientist Jobs in Zug
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Suchergebnisse - Clinical Scientist Jobs in Zug
Leadless Clinical Specialist (m/f/d) Cardiac Rhythm Management - region Switzerland, Austria, Poland
Abbott Laboratories-Zug
mothers, female executives, and scientists.
Abbott Medical is looking for a
Leadless Clinical Specialist (m/f/d) Cardiac Rhythm Management - region Switzerland, Austria, Poland
to be based in Switzerland
PURPOSE OF THE JOB
As Leadless Clinical...
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European Medical Writers Association (EMWA)-Zug
will involve crafting scientific and regulatory documents, collaborating with cross-functional teams to ensure adherence to the highest quality standards. Specifically, you'll be responsible for creating and maintaining Clinical Evaluation Reports (CERs...
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Roche-Zug
and external developments, trends, and other dynamics in Infectious Diseases (TB, Hepatitis, HIV and HPV) and maintain the highest levels of scientific and clinical knowledge in Infectious Diseases (TB, Hepatitis, HIV, and HPV).
People Leadership
• Ensures...
GSK-Zug
disease area.
Preferred Qualifications & Skills:
Advanced Scientific Degree (Ph D, MD, Pharm D).
Knowledge of the drug development process in regulatory affairs.
Awareness of global regulatory processes, including submission and approval activities...
GSK-Zug
will be the overall leader of the non-interventional data generation team for the Oncology therapy area. Accountabilities include management and development of a team of leaders and scientists with expertise in real-world evidence and other non-interventional study...
Roche-Zug
process and present this data to clinicians, researchers, and caregivers to improve research outcomes and patient care by offering a suite of Clinical Decision Support (CDS) solutions.
As a Principal Quantitative Scientist, you are responsible for leading...
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Cytokinetics-Zug
as implementation of post-marketing requirements.
The Senior Director, Regulatory Affairs Europe will work closely with the Global Regulatory Lead and be a member of the Global Regulatory Team. The individual will work cross-functionally including with Clinical...
GSK-Zug
will be the overall leader of the non-interventional data generation team for the Oncology therapy area. Accountabilities include management and development of a team of leaders and scientists with expertise in real-world evidence and other non-interventional study...
Blueprint Medicines-Zug
Bachelor's degree; advanced scientific related degree a plus
• A minimum of 3-5 years of regulatory drug development experience and a minimum of 2 years of direct regulatory affairs experience
• Pharmaceutical industry experience essential
• Experience...
GSK-Zug
portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders so as to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships...
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Johnson & Johnson-Zug
technical troubleshooting and relevant scientific clinical literature and new product information.
• Prioritize and appropriately respond to requests in a high-pressured, stressful environment, maintain composure and focus whilst problem solving in stressful...
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Johnson & Johnson-Zug
for the therapeutic area (TA) including treatment trends, unmet medical needs, scientific insights and clinical studies to enhance company product value through high quality scientific knowledge management.
• Close collaboration with key Leading Specialists...
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Roche-Zug
Responsibilities
• Supporting the team with medical/scientific expertise to help develop novel diagnostics solutions.
• Conduct comprehensive literature reviews, collation of relevant clinical and scientific information from different sources, and create new...
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Roche-Zug
Want to find out more about our site? Then watch this video.
You will join the Scientific Communications Team within Medical Affairs, which is one of the three functions that make up the Clinical Development and Medical Affairs department within Roche...
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Roche-Zug
clinical and scientific information from different sources, and create new scientific content.
• Writing a wide range of medical and scientific documents.
• Collaborate with other functions as well as external experts on development programs.
• Support...
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