interaction Jobs in Basel

Sobi is an international biopharmaceutical company, dedicated to providing access to innovative treatments that transform life for people with rare diseases in the areas of haematology, immunology and specialty care. With our head office in Stockholm, Sweden, Sobi also has premises in Basel, Switzerland. You can find more information about Sobi at The...

Work Selection AG is seeking a Regulatory Specialist (CMC) for a 12-month assignment in Basel, supporting Roche's early clinical development programs. The role focuses on handling Health Authority interactions, including IND, IMPD, and related CTAs, with emphasis on IMPs and early development.You will collaborate with global teams, maintain Veeva-based CMC...

Gi Group is seeking a Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR) to lead global regulatory submissions and manage CMC information for IND, IMPD, and NDA/BLA/MAA filings. The role collaborates with affiliates, policy teams, and partners on early clinical stage programs and IMPD submissions.The ideal candidate has 3–4 years of CMC...

The Opportunity We are offering a unique opportunity for a hands‑on NMR Expert in our Analytical Molecular Characterization group. As a Centre of Excellence for Analytics, we provide state‑of‑the‑art methods and services for determining chemical structures, purities, and impurities, supporting portfolio projects throughout the entire value chain. In...

h3Clinical Trial Psych Rater - German Speaking /h3 pbLocation: /b Remote/Virtualbr/bHours: /b Estimated 10-16 hours per monthbr/bRole: /b Clinical Specialist /p h3About IQVIA /h3 pIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. The Medical Director Hemato-Oncology, Medical...

pBeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. /ppThe Country Medical Director Switzerland is the...

Our client is a global leader in the pharmaceutical industry, committed to advancing science and delivering innovative therapies to patients worldwide. To support ongoing clinical development activities, we are looking for a Regulatory Specialist (CMC) with experience in early-stage development and clinical regulatory submissions.In this role, you will...

pRoche is offering a two-year Early Talent program in Regulatory Affairs that blends hands-on assignments with tailored learning. It provides exposure to the full lifecycle of pharmaceutical products and rotating opportunities within PDR. /ppETs work with global teams, developing scientific writing skills and preparing regulatory documents for Health...

For our CMF (Craniomaxillofacial) business in Basel, we are looking for an experienced Senior Global Product Manager. In this role, you will take ownership of a global product segment throughout its entire lifecycle – from developing the product strategy and new products to international launches and the continuous development of the existing portfolio.You...

Roche Pharma Research & Early Development (pRED) Basel invites you to join a 6-month internship to explore how large language models can automate lab workflows. You will connect LLMs to laboratory equipment and software, enabling natural language interactions and automated tasks. You'll evaluate tools, develop a PoC with a liquid handling system, run tests,...

pBeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. /p /brpThe Country Medical Director Switzerland is...

OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings. This...

Research Assistant/Technician (Laborant:in) 60%As a joint venture of the University of Basel and the University Hospitals Basel, the Department of Biomedicine (DBM) brings together basic and clinical scientists to advance the understanding of health and disease.We are home to more than 67 research groups and over 800 employees across six locations in the...

In the position of Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR), you will be accountable for handling all Health Authority interactions pertaining to CMC Information (for example in an IND, IMPD and NDA/BLA/MAA filings), as well as informational and/or pre-submission meetings with global Health Authorities, partners and industry experts....

Adecco Switzerland seeks a Senior HEOR Manager to drive COA strategies across international programs, ensuring patient voice integration in development, HTA submissions, and regulatory interactions.You will lead COA projects, coordinate with Clinical Development, Medical Affairs, and Regulatory teams, and manage external partners, with a focus on COA/PRO...

Strategic Direction: Design and implement European regulatory pathways that seamlessly align with worldwide clinical development roadmaps.Health Authority Interface: Act as the primary regional liaison for the European Medicines Agency (EMA) and coordinate communications with various national competent authorities across Europe.Agency Meetings: Direct the...

ppNotre client, une entreprise biopharmaceutique internationale basée à Bâle, développe et fabrique des biologics et petites molécules pour des marchés soumis à EU/FDA/Swissmedic. Pour renforcer l’équipe Regulatory CMC, nous recherchons un(e) Responsable Affaires Réglementaires CMC capable de piloter la stratégie dossier de la clinique au...

pThe Associate Director, bHead of Quality Assurance Fachtechnisch verantwortliche Person (FvP) /b, is responsible for leading the Quality function of Accord Healthcare AG Switzerland and ensuring full compliance with Swiss pharmaceutical regulations, Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), narcotics legislation, and all...

ppRevolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s RD pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor;...