20 basel English-speaking jobs in Riehen

foratalentedProcurement Lead to join our industry leading Project Delivery and Construction team at our growing Basel

For our client, a pharmaceutical company in Basel, we are looking for a qualified, experienced and motivated

Senior Expert/Functional Lead (Biologic Drug Products) Job ID REQ-10054681 Summary Location: Basel, Switzerland ... You will be working in an international team, located at our headquarters in Basel, Switzerland, focusing

Flow Cytometry Specialist • Basel-Stadt, Switzerland #J-18808-Ljbffr

Senior Global Program Safety Team Lead - Immunology Job ID REQ-10055040 Summary Are you ready to lead with excellence and make a significant impact on our company's safety surveillance strategy? We are looking for a dynamic and strong people manager to design and develop our safety surveillance strategy for product approval.

Director Data & Digital Strategy (Biomedical Research) Job ID REQ-10054625 Summary This key director for strategy role will enable and drive the creation of the data & digital strategy for Biomedical Research in alignment with the Novartis AI strategy and will ensure execution of it by designing the required strategic initiatives driven by the Data & Digital Office.

Job ID REQ-10027583 Summary We’re a team of dedicated and smart people united by a drive to achieve together. You will drive portfolio policy for Oncology and shape an industry-leading policy strategy to create an optimal policy environment for key Novartis portfolio assets.

Responsibilities: Digital Transformation: Several years of architecting key initiatives and acting as a digital translator between business needs and technical roles by navigating across both domains seamlessly. Strategic and analytical thinker capable of applying lean and digital principles. Conducting use case prioritization and assuming product owner role.

Who We Are TetraScience is the Scientific Data and AI Cloud company. We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes.

Job ID REQ-10051302 Summary Working primarily within our Diseases of Ageing and Regenerative Medicine (DARe) department at Biomedical Research, this Senior Principal Scientist role will lead in-vivo Imaging with the aim to deliver groundbreaking imaging techniques and technology to support and further Drug Discovery across our key research Disease Areas, including Oncology, Immunology, Neuroscienc

Proclinical is seeking a dynamic individual for a global project management role within the Clinical Supply Chain. This position focuses on ensuring the timely planning and execution of supply strategies to maintain the continuous supply of clinical finished goods to patients.

Job ID REQ-10054112 Summary The Global Program Clinical Head (GPCH) in CVM is the global clinical leader responsible for one or more clinical programs across indications, involving one or multiple compounds.

Track record of successfully working with other functions Location: This role is based in Basel, Switzerland

#Hybrid Location: Basel, Switzerland About the Role Key Responsibilities: Provide outstanding partnering

Job Description Summary The Clinical Operations Program Head (COPH) is accountable to deliver data-driven, actionable operational and strategic insights for execution of a clinical development program and all associated trials by representing GCO at the Global Clinical Team (GCT) as well as at the Global Program Team (GPT).

Location: Basel Start date: ASAP Key Responsibilities: Lead the technical design and implementation of

Manufacturing Science and Technology department (MSAT), you will contribute to the MSAT team at the Basel

Duration: 1 year Ready to travel internationally - Europe, US, APAC- -% The CTSM serves as a broker role between study vendors involved in IMP packaging and further management (e. g.

Contract duration: 1 year Responsibilities: Overseeing the creation, maintenance, and quality of the Trial Master File, a collection of essential documents for a clinical trial and TMF archival Ensuring TMF documents are accurate, complete, and compliant with regulations (e. g. , ICH/GCP) and internal/external SOPs.

Tasks and Responsibilities: Provide 1st level IT support to customers and acts as a single point of contact, for incident, request and customer service queries, via phone, email, chat or face-to-face Incident Management: assisting customers and endeavouring to resolve their issues as effectively as possible, collaborating with other colleagues when required.