Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
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
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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ITech Consult AG-Basel
Regulatory Specialist - Clinical or Early-Stage Development
Regulatory Specialist - Clinical / Early-Stage Development (CMC Focus) : CMC / IMPs / Clinical Trial
Applications (CTAs) / Change Control / Deviation Management /Change controls / CMC...
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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
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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Universität Zürich-Zurich
trial portfolio, monitoring milestones and resources, and reporting progress to management and governance bodies.
• Recruiting, supervising and supporting the development of a veterinary nurse dedicated to clinical trial activities.
• Contributing...
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stellen-zuerich.ch -
Syneos Health Switzerland GmbH-Schweiz
Syneos Health Switzerland is seeking a Site Activation Manager to lead site start-up activities across sponsor partnerships in Switzerland. You will collaborate with Business Development, Contracts, Clinical and Data Management teams to drive...
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PSI-Zug
Job Description
At PSI CRO, our Regional Project Leads are trusted leaders who drive the successful delivery of clinical trials across multiple countries. You'll partner with Project Managers, CRAs, sponsors, and cross-functional teams to ensure...
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University of Bern-Bern
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...
Read more
stellen-bern.ch -
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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ITech Consult AG-Basel
Regulatory Specialist - Commercial/Post-Marketing & Remediation
Regulatory Specialist - Commercial / Post-Marketing & Remediation :CMC / IMPs / Clinical Trial Applications (CTAs) / Change Control / Deviation Management /Change controls / CMC...
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ITech Consult AG-Basel
Regulatory Specialist: CMC / IMPs / Clinical Trial Applications (CTAs) / Change Control / Deviation Management /Change controls / CMC regulatory / Veeva Document Management / Post-Marketing / Remediation/ English / Deutsch
Background
A healthier...
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ITech Consult AG-Kaiseraugst
Organization (GCSC) is responsible for the cost-effective and timely production of investigational medicinal products (IMPs), ensuring that no clinical trial is delayed and that every patient receives high-quality treatment.
The Site SHE Coordinator...
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Alentis Therapeutics-Allschwil
Operations to ensure efficient trial conduct.
• Collaborate with Biostatistics and Data Management on data analyses and interpretation.
• Partner with Translational Medicine and Biomarker teams to integrate scientific insights into clinical development...
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join.com -
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 -
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