Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
IQVIA-Basel-stellen-basel.ch-
The Senior Clinical Supply Chain Manager is responsible for leading the strategic planning, oversight, and delivery of a portfolio of clinical supply chain projects, ensuring the effective and timely provision of clinical trial supplies across...
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BeiGene, Ltd.-Basel-appcast.io-
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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Novartis-Basel-stellen-basel.ch-
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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Medidata Solutions, Inc.-Basel-appcast.io-
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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Roche-Basel-roche.com-
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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IQVIA-Basel-appcast.io-
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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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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BeiGene, Ltd.-Basel-appcast.io-
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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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-stellen-basel.ch-
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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Roche-Basel-roche.com-
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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Skyvor Med-Basel-stellen-basel.ch-
and deploy advanced digital platforms, including electronic Case Report Forms (eCRFs) and workflow management systems.
• Process Automation: Design and implement AI and automation solutions to improve the efficiency of clinical trial workflows and operations...
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Roche-Basel-roche.com-
processes and the highest scientific standards—utilising deliverables based on advanced data science, pharmacoepidemiology methodologies, and literature queries across Real World Data, Clinical Trial data, and literature databases while staying abreast...
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BeiGene, Ltd.-Basel-stellen-basel.ch-
ideas on how to deliver on clinical trials are generated and considered
Quality
Line management responsibilities: Ensures team members are trained on and are adhering to required processes and SOPs Promotes a quality mindset in the regional study...
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Roche-Basel-roche.com-
independently develop, validate, and maintain datasets and statistical outputs for clinical trials, including Study Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs), ensuring programming...
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