Drug Safety Trainee

Our client Skyhawk is a clinical-stage biotechnology company developing novel small molecules designed to modulate RNA processing of disease targets, including those traditionally thought to be “undruggable,” and yield therapies for some of the world’s most intractable diseases. They have built a sophisticated, integrated proprietary platform that...

Our client Skyhawk is a clinical-stage biotechnology company developing novel small molecules designed to modulate RNA processing of disease targets, including those traditionally thought to be “undruggable,” and yield therapies for some of the world’s most intractable diseases. They have built a sophisticated, integrated proprietary platform that...

Our client Skyhawk is a clinical-stage biotechnology company developing novel small molecules designed to modulate RNA processing of disease targets, including those traditionally thought to be “undruggable,” and yield therapies for some of the world’s most intractable diseases. They have built a sophisticated, integrated proprietary platform that...

Our clientSkyhawk is a clinical-stage biotechnology company developing novel small molecules designed to modulate RNA processing of disease targets, including those traditionally thought to be “undruggable,” and yield therapies for some of the world’s most intractable diseases. They have built a sophisticated, integrated proprietary platform that...

Our client Skyhawk is a clinical-stage biotechnology company developing novel small molecules designed to modulate RNA processing of disease targets, including those traditionally thought to be “undruggable,” and yield therapies for some of the world’s most intractable diseases. They have built a sophisticated, integrated proprietary...

**Salary**: CHF170000 - CHF190000 per annum**Job type**: Permanent **Location**: Basel, Switzerland **Function**: PVG & Drug Safety, Global Drug Safety **Posted**:28/06/2023 **Ref**: BBBH22928 - Hi I'm Nyvine , I manage this role Hobson Prior are seeking for a Global Product Safety Science Lead to join a brilliant biopharmaceutical organisation on a...

391327BR **Global Program Safety Lead - Immunology**: Switzerland **About the role** The GPSL ensures optimal patient safety and leads the integration, analysis and interpretation of internal and external safety information from all sources through lifecycle management. This position reports to the Head Patient Safety Immunology. **Key...

Do you want to join VecturaFertinPharma (Philip Morris)? We're looking for a: **Your mission** Duration : open-ended contract through Manpower Location : Basel or Neuchâtel or Remote In this role as Clinical Safety Physician you are responsible for implementing and overseeing all areas of safety monitoring and reporting for clinical trials for Vectura...

Role & Function The Global Product Safety Science Lead is a key role within Global Pharmacovigilance (PV) and Patient Safety. You will be leading the safety surveillance activities for assigned marketed Sobi products and for products under development. As part of our PV team, you will be working collaboratively with other PV functions to ensure that safety...

2023 will see Sandoz become a standalone organization! As a global market leader in Generics and Biosimilar medicine, Sandoz is stepping forward from a position of strength! Those joining Sandoz in the coming months will help shape the future of the company, it’s growth, innovation, culture and how Sandoz impacts the lives of millions. These will be...

**Salary**: CHF150000 - CHF165000 per annum**Job type**: Permanent **Location**: Basel, Switzerland **Function**: Technical Operations, Quality Control, Chemist **Posted**:05/05/2023 **Ref**: BBBH22209 - Hi I'm Christopher , I manage this role Hobson Prior are seeking for a CMC Lead Drug Substances to join a fantastic biotech establishment on a...

**Company Description**: - Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic...

**Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere.** **CMC Lead Drug...

At this position, you are part of the Regulatory Affairs and Pharmacovigilance Team within the Medical Department of the Swiss affiliate at CSL Vifor (no direct reports). You are the main responsible person for independently processing drug safety reports for our products. You perform your tasks in collaboration with other colleagues of the same team as well...

**Drug Substance CMC Lead** Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic...

**About Idorsia Pharmaceuticals Ltd** Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core. Headquartered in Switzerland - a European biotech hub -...

**_The Life Science Career Network_** **International PV Business Process Leader** Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare. As the world's largest R&D spender in the pharmaceutical and diagnostics domain, they work in a vast number of drug discovery & therapeutic areas and are highly...

The purpose of the role is to lead the Clinical Development Team and work with all centrally managed groups, including Clinical Operations, Regulatory, Safety, Preclinical and CMC teams, to efficiently develop new drugs and manage Life Cycle programs of marketed drugs, in line with the agreed strategy for the Rare Diseases business and in compliance with all...

**The Life Science Career Network** Our client, a pioneer in Drug Discovery and Development and a leader in Personalized Healthcare, stands at the forefront of innovation. As the world's largest R&D spender in the pharmaceutical and diagnostics domain, they operate across a wide spectrum of drug discovery and therapeutic areas, earning global...

500! The number of regulatory documents we authored last year. As a Regulatory Writer you will write and review high quality clinical and safety documentation for submission to regulatory authorities. **Location**: Basel, Switzerland #LI-Hybrid **Your responsibilities**: Your responsibilities include, but are not limited to: - To author and review high...