Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
gloor & lang ag-Basel
Senior Clinical Outcomes Assessment (COA/PRO) Manager – HEOR
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...
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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...
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Work Selection-Basel
IMPDs)
• Experience with Clinical Trial Applications for early- to mid-stage development programs
• Solid hands-on experience with Veeva Document Management for regulatory submissions
• Fluent English, written and spoken, minimum C1
Nice to Haves...
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CTC Resourcing Solutions AG-Basel
contributes to the design, conduct, analysis, interpretation, and reporting of clinical pharmacology trials across drug development. The role provides scientific and medical input to trial teams, supports protocol and trial document development...
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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...
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appcast.io -
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...
Read more
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...
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jobcourier.ch -
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...
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BeiGene, Ltd.-Basel
a thorough understanding of global regulatory requirements and guidelines governing the conduct of clinical trial operations across multiple regions.
Supervisory Responsibilities:
Not Applicable
Computer Skills:
All basic Microsoft Office Programs
Other...
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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...
Read more
join.com -
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...
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appcast.io -
ELAN Personal AG-Basel
trials, IMPD preparation, and clinical regulatory submissions
• Hands-on experience with Veeva Document Management for Regulatory submission
• Experience with Clinical Trial Applications for early to mid stage programs
Position 2: Regulatory Specialist...
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IQVIA-Basel
IQVIA LLC in Basel, Switzerland seeks a Systems Design Project Manager to support clinical trials by designing and delivering IRT systems. You will analyze study protocols, consult with clients, and manage project timelines, ensuring compliance...
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stellen-basel.ch -
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...
Read more
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...
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