Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
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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Universität Bern-Bern-
stakeholders, including CEC, DSMB groups, and contribute to continuous improvement of processes.
• Vendor and CRO oversight.
Requirements
• Master's degree in a health or life science-related field; advanced degree or certificate in clinical trial management...
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Michael Page (Switzerland)-Geneva-appcast.io-
Strong experience negotiating and managing:
• Clinical Trial Agreements (CTAs)
• CRO Agreements
• Research-related agreements
• Data Protection and Privacy Agreements
• Demonstrated experience working on multi-jurisdictional matters within...
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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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BeiGene, Ltd.-Schweiz-appcast.io-
Excel, PowerPoint) **Preferred Qualifications:*** Certification in GCP auditing or clinical research is a plus.* Experience working with electronic Trial Master File (eTMF) and Clinical Trial Management Systems (CTMS).* Familiarity with risk-based...
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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...
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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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Rivia SA-Zurich-appcast.io-
Rivia is a data engine for clinical trial intelligence. It provides data infrastructure and AI-driven workflows for clinical trial teams, enabling biotechs to run studies more efficiently and to demonstrate which patients derive the greatest benefit...
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Bristol Myers Squibb-Boudry-
of patients, and the careers of those who do it.
What if the next clinical trial you shaped went on to change how a disease is treated - forever?
That's not a hypothetical here. At Bristol Myers Squibb, it's the everyday reality for the scientists who sit...
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CTC Resourcing Solutions AG-Basel-stellen-basel.ch-
Data Management activities 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...
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BeiGene-Basel-
of clinical operations knowledge, organisational skills, project management and leadership competencies.
• Adheres to ICH/GCP, assure clinical trial protocols are executed at clinical trial sites in accordance to ICH guidelines and GCP, local regulations...
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University of Bern-Bern-stellen-bern.ch-
to continuous improvement of processes.
• Vendor and CRO oversight.
Requirements
• Master’s degree in a health or life science-related field; advanced degree or certificate in clinical trial management/coordination or regulatory affairs is an asset...
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Johnson and Johnson-Allschwil-
Preferred Knowledge, Skills and Abilities:
• Knowledge of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and/or Good Pharmacovigilance Practice (GPvP)
• Experience with fundamentals of clinical trial risk management
• Global clinical...
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Swiss Cancer Institute-Bern-
research for a cure tomorrow,” we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the pharmaceutical industry. Approximately 70 employees at our Competence Center in Bern work closely with all...
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Work Selection AG-Basel-jobcourier.ch-
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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