Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
Universitätsspital Basel-Basel
Lab Technician / Clinical Trial & Biobanking Coordinator
Es gibt viele Gründe, zu uns zu kommen: Am USB arbeiten heisst in erster Linie, Teil eines engagierten Teams aus über 7500 Mitarbeitenden aus rund 90 Nationen zu sein. Unser lebhafter Alltag...
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Novartis-Basel
Management, Clinical Development, Clinical Research, Clinical Trial Implementation, Clinical Trial Process, Clinical Trials, Digital Marketing, Digital Strategy, Innovation, Innovative Solutions, Patient Recruitment, Pharmaceutical Industry...
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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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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...
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roche.com -
Medidata Solutions, Inc.-Basel
engagements with complete autonomy. Partnering directly with Client Executives (CEs) and Customer Success Managers (CSMs), you will form a powerful account triad to drive complex clinical trial technology sales cycles within mid-market biopharma accounts...
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CTC Resourcing Solutions-Basel
for assigned clinical trials, ensuring high-quality, consistent data delivery in line with internal standards, applicable regulations, and agreed timelines. The role coordinates eCRF development, data review and query management, database lock, and SDTM-related...
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IQVIA-Basel
Systems Design Project Manager – IRT Basil, Switzerland
About the Role
The Systems Design Project Manager (IRT) plays a key role in supporting clinical trials by designing and delivering IRT systems that ensure patients receive the correct study...
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ITech Consult AG-Basel
for risk management activities including preparation and maintenance
of CCDS, labeling document maintenance (including IB), risk communications, RMP.
• Review of clinical protocols, study reports, Investigator’s Brochure (IB), informed consent form (ICF)
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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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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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Sobi-Basel
and appropriate Sobi RDMA functions, this role has a strategic leadership to drive best practices for clinical trial operations, clinical trial systems and clinical trial vendor management.
Functional leadership and team management
• Lead the PV Partnership...
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Roche-Basel
to bring the power of sensor measures to patients everywhere: in clinical drug trials and clinical care.
We drive research, workflows and analytics for Digital Biomarkers and Remote patient management in Roche Information Solutions. Together with our...
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roche.com -
BeiGene, Ltd.-Basel
degree; JD highly preferred or 8+ years of outstanding experience managing and negotiating clinical trial agreements and budgets
• Experience in the CRO or pharmaceutical industry is essential.
Other Qualifications
• Good knowledge of ICH-GCP...
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stellen-basel.ch -
Roche-Basel
with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging...
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roche.com -
IQVIA LLC-Basel
IQVIA LLC seeks a Systems Design Project Manager for IRT Basil, Switzerland, to design and deliver IRT systems for clinical trials. You will work with sponsors to translate study requirements into system specs, oversee implementation, and manage...
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