Expert Regulatory Writer

500! The number of regulatory documents we authored last year. As an Expert Regulatory Writer you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinical Summaries, Clinical Overview, Briefing Books, answers to Health Authority...

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...

This is an exciting opportunity for a Clinical Science Enabler to join Hobson Prior International Ltd's team. The successful candidate will be responsible for supporting drug development from start to finish, ensuring that new medicines reach patients quickly and safely.About the Role:Plan and manage clinical studies to ensure data accuracy and compliance...

**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.** **Principal Medical...

**About the role**: Takeda’s Neuchatel Manufacturing Sciences/Quality Compliance teams are looking for a highly motivated Technical Writer. The role is expected to have a solid understanding of regulatory guidelines as well as background of biopharma processes including related GMP requirements. **How you will contribute**: **Your mission** As Technical...

**Job Title**: Medical Writer (Oncology) 12-month contract **Reports to (Title)**: VP Clinical Development Oncology **Location**: Europe **Direct Reports**: No **Department**: Clinical Development The Hengrui ex-China organization drives the development and commercialization of the Hengrui innovative medicines portfolio for the US, Europe and Japan. Our...

Job Title: Medical Writing Expert (Regulatory Documents)    TN Switzerland is seeking a seasoned Medical Writing Expert with expertise in regulatory documents to join our team.About the RoleWrite clear and concise clinical submission documents, including clinical study reports, protocols, clinical overviews, investigator brochures, and summary...

TN Switzerland is committed to developing and maintaining high-quality regulatory processes that ensure patient access to innovative treatments. We are seeking a highly skilled Regulatory Expert to join our team as a Global Regulatory Expert - Clinical Studies.In this role, you will be responsible for leading the clinical trial regulatory strategy and...

About the CompanyRm IT Services GmbH is a globally operating Basel-based company in the Pharma sector. We are committed to delivering high-quality products and services, and we are seeking a highly skilled and motivated professional to join our team.Job DescriptionDesign, plan, supervise, and monitor all activities of assigned pipeline early and late phase...

At Julius Baer, we celebrate and value the individual qualities you bring, enabling you to be impactful, to be entrepreneurial, to be empowered, and to create value beyond wealth. Let’s shape the future of wealth management together. Are you an experienced regulatory change expert, which is passionate about the transformation of our industry? In this...

**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 -...

At Julius Baer, we celebrate and value the individual qualities you bring, enabling you to be impactful, to be entrepreneurial, to be empowered, and to create value beyond wealth. Let’s shape the future of wealth management together. Are you an experienced regulatory change expert, which is passionate about the transformation of our industry? In this...

Job RequirementsWe are seeking an experienced Regulatory Affairs professional to join our team as a Senior Regulatory Affairs Consultant. The successful candidate will have a strong background in regulatory affairs within the medical device and pharmaceutical industries, with a focus on FDA processes.Key ResponsibilitiesThe ideal candidate will be...

**Quality Product Expert - 8 Month Contract** **About the role**: The objective of this position is to provide expertise and appropriate documentation needed for the life cycle of the products being produced entirely or partially in the Neuchâtel facility for routine activities and improvement initiative projects. The job holder will be part of the Quality...

About UsExponent is a global leader in providing expert consulting services to clients in the industrial chemicals sector. Our team of experts has extensive experience in managing regulatory projects and providing technical and regulatory consultancy services.Job DescriptionThe successful candidate will be responsible for managing REACH regulatory projects,...

Why Abbott Laboratories?At Abbott Laboratories, we empower people to live more fully at all stages of life. Our diverse portfolio and innovative solutions make us a leader in healthcare. As an Associate Director Regulatory Affairs Biosimilars, you will lead the development and execution of the global regulatory strategy for biosimilar/biotech products,...

Do you want to join us on the journey of disrupting the spend management business? Do you like to work in a fast-paced environment with a passionate and supportive team? Yokoy is growing! We recently closed our $26M Series A funding and are entering a fast-paced Hypergrowth phase. We're now looking for a new colleague to become our UX Writer! Yokoy is an...

We have an exclusive mandate for one of our clients in Medical Devices based in Canton of Neuchatel. As a Regulatory Affairs Manager, you will be responsible for: - Support new product development by using in-depth knowledge and understanding of US domestic and international medical device, regulations (including 510k, and International dossiers) - Lead...

Key ResponsibilitiesThe Clinical Pharmacology Science Specialist will be responsible for the following key activities:Contributing to clinical pharmacology aspects of patient studiesIdentifying solutions for clinical study supportUtilizing advanced data visualization tools to facilitate data-driven decision-makingEnsuring regulatory complianceWriting final...

WillHire is seeking a highly skilled Senior Analytical Expert to join our regulatory compliance team.Job Responsibilities:Develop and implement regulatory compliance strategies.Supervise and monitor project activities.Communicate effectively across organizational interfaces.Lead the transfer of know-how or procedures to other departments or external...