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Clinical Trial Manager Jobs in Basel

1 - 15 of 24
1 - 15 of 24
Search Results - Clinical Trial Manager Jobs in Basel
ITech Consult AG-Basel
Regulatory Specialist - Clinical / Early-Stage Development (CMC Focus) : CMC / IMPs / Clinical Trial Applications (CTAs) / Change Control / Deviation Management /Change controls / CMC regulatory / Veeva Document Management / Post-Marketing...
Adecco-Basel
Shape the future of patient-centered drug development For our client, a global leader in the life sciences industry, we are looking for an experienced Senior HEOR Manager to drive Clinical Outcome Assessment (COA) strategies across international...
Work Selection AG-Basel
Investigational Medicinal Product Dossiers (IMPDs) and Clinical Trial Applications (CTAs). The role requires strong technical CMC regulatory expertise, close collaboration with global stakeholders and proficiency in Veeva Document Management to support compliant...
appcast.io -
ITech Consult AG-Basel
Regulatory Specialist - Commercial / Post-Marketing & Remediation :CMC / IMPs / Clinical Trial Applications (CTAs) / Change Control / Deviation Management /Change controls / CMC regulatory / Veeva Document Management / Post-Marketing / Remediation...
F. Hoffmann-La Roche AG-Basel
in life sciences), backed by proven and relevant operations experience, a strong working knowledge of drug development processes and regulations (including ICH/GCP guidelines). Clinical trial management experience is preferred. Act as a results-driven self...
appcast.io -
Adecco-Basel
Shape the future of patient-centered drug development For our client, a global leader in the life sciences industry, we are looking for an experienced Senior HEOR Manager to drive Clinical Outcome Assessment (COA) strategies across international...
stellen-basel.ch -
BeiGene, Ltd.-Basel
and selected New Markets, in alignment with global R&D Legal strategy and company priorities.- Advise on the design, start-up and conduct of clinical trials and other human-subject research, including informed consent, ethics committee requirements, patient...
appcast.io -
Hays-Basel
such as LangGraph, CrewAI, or AutoGen to automate complex clinical data management tasks  •  Build collaboration systems where specialised agents (, Planner, Validator, and Protocol Reviewer) resolve end-to-end data challenges through high-quality, testable code...
Novartis AG-Basel
faster. As Innovation Capability Director – Global Clinical Operations, you will lead the identification, implementation and scaling of innovative recruitment and patient engagement solutions that improve clinical trial participation around the world...
stellen-basel.ch -
Proclinical-Basel
technical regulatory submissions for clinical and commercial products, ensuring compliance with local and regional requirements.  •  Oversee the regulatory lifecycle management of assigned products, including evaluating change records and maintaining CMC...
IQVIA-Basel
experience in clinical operations roles plus minimum 6 years’ experience in a GCP compliance or equivalent role (i.e. quality) including people management experience (minimum 4 years).  •  Experience in oncology global trials is preferred.  •  Requires deep...
appcast.io -
ITech Consult AG-Basel
Regulatory Specialist – Commercial / Post-Marketing & Remediation :CMC / IMPs / Clinical Trial Applications (CTAs) / Change Control / Deviation Management /Change controls / CMC regulatory / Veeva Document Management / Post-Marketing / Remediation...
BeiGene, Ltd.-Basel
the same or similar indications and will collaborate closely with global cross-functional teams incl. HEOR, Medical, commercial, clinical development and regulatory as well as seek input and alignment with affiliate teams to develop strategy and access...
appcast.io -
gloor&lang AG-Basel
 12.  month temporary assignment | Basel | Global Pharmaceutical Company For a global pharmaceutical company in Basel, we are looking for an experienced Senior Clinical Outcomes Assessment (COA/PRO) Manager with strong expertise in patient-centered...
join.com -
Roche-Basel
Alzheimer’s disease, neurodevelopmental disorders and multiple sclerosis. MD degree and medical monitoring experience in phase 1-2 clinical trials will be considered a major plus. The Opportunity  •  Shape the future of global Phase 0–2 studies...
roche.com -
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