Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
Octapharma AG-Lachen
Clinical Trial Manager - Central Monitoring
Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers...
Randstad (Schweiz) AG-Lausanne
study execution in line with relevant pharmaceutical
standards.
Responsibilities
• Support
the Clinical Project Manager(s) in study execution, including
tracking study milestones and key
deliverables
• Maintain and
manage the Trial Master File (TMF...
Michael Page Switzerland-Lausanne
GCP guidelines and clinical trial lifecycle- Experience with eTMF and TMF- Exposure to outsourced clinical study models or vendor oversight- Excellent organizational and management skills- Strong attention to detail with the ability to manage multiple...
SJP Biotec GmbH-Zurich
development strategy across one of the most compelling areas in the current oncology drug development field - RAS/eIF4A/translation-pathway inhibition.TasksTranslate and deliver key directives from the board and senior management, and serve as the clinical...
Michael Page Switzerland-Lausanne
Senior Clinical Trial AssistantIl Senior Clinical Trial Assistant fornisce supporto operativo essenziale in tutte le fasi degli studi clinici. Questo ruolo garantisce la conformità agli standard di alta qualità e il corretto svolgimento delle...
CH_Prog_Partner_Whatjobs_Mixed_CPC-Schweiz
development strategy across one of the most compelling areas in the current oncology drug development field - RAS/eIF4A/translation-pathway inhibition.TasksTranslate and deliver key directives from the board and senior management, and serve as the clinical...
Michael Page Switzerland-Lausanne
guidelines, clinical trial lifecycle, and sponsor responsibilities Experience working on both sponsor and/or CRO sides, with the ability to effectively collaborate across stakeholders Strong data management skills, including collection, review, and analysis...
BeiGene, Ltd.-Basel
of vendor management and GCP audit activities to ensure compliance with GCP regulations.This role ensures that clinical trials and all vendors adhere to internal quality standards, regulatory requirements, and contractual agreements, thereby supporting...
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CH_Prog_Partner_Whatjobs_Mixed_CPC-Bern
development strategy across one of the most compelling areas in the current oncology drug development field - RAS/eIF4A/translation-pathway inhibition.TasksTranslate and deliver key directives from the board and senior management, and serve as the clinical...
C028 (FCRS = CH028) Novartis Pharma AG-Basel
information. Please include the job requisition number in your message.
Skills Desired
• Clinical Research
• Clinical Trials
• People Management
• Program Management
• Regulatory Compliance
• Resource Management (Organizational)
• Risk Management
#J-18808...
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MSD Malaysia-Zurich
and study managers to lead/support clinical trial scientific activities.**Job Responsibilities:*** Responsible for the clinical/scientific execution of clinical protocol(s).* Serves as the lead clinical scientist on the clinical trial team.* Collaborates...
Manpower Basel-Basel
and compliance of clinical trial materials across the global supply chain. The team provides QA oversight for the global IMP Distribution Network and works closely with key stakeholders in Global Clinical Supply Chain Management Distribution.
This position offers...
Viatris-Allschwil
Manager (m/f/d) role will make an impact:
Lead and ensure compliance of global CQA processes across multiple sites
Act as key Quality partner for cross-functional stakeholders (e.g. Clinical Trial Teams, Biometry, CROs)
Drive continuous improvement...
SJP Biotec GmbH-Zurich
development field - RAS/eIF4A/translation-pathway inhibition.
Key Responsibilities
Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
Lead and manage all clinical development activities...
Bristol-Myers Squibb-Boudry
programs and/or indications (e.g., data standards, programming specifications, statistical analysis plans).
• Lead lessons learned communication and ensure alignment to avoid unnecessary amendments.
• Act as Trial Lead for complex clinical studies when...
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