Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
Coopers Group AGBasel
Clinical Trial Manager
m/f/d, Basel-Stadt
The Clinical Trial Manager serves as their region's lead and expert on complex clinical development trials to secure expeditious country level set-up, start, enrolment and quality control
Contract duration...
1 similar job: Zürich
Michael Page SwitzerlandLausanne
at the forefront of science and health.They offer a dynamic and international working environment focused on excellence and continuous improvement.DescriptionSupport Clinical Project Managers in tracking study milestones and deliverablesMaintain and oversee Trial...
Randstad (Schweiz) AGLausanne
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/eTMF), performing periodic completeness...
nemensis agBaseljobup.ch
Clinical Trial Supply Manager (m/w/d)
Shape the future of clinical supply chains your expertise keeps patients supplied.
• ? Duration: 18-month contract (extension possible)
• ? Location: Basel, Switzerland
• ? Employment type: Temporary
About...
Michael Page SwitzerlandLausanne
The Senior Clinical Trial Assistant provides essential opera
Senior Clinical Trial Assistant
The Senior Clinical Trial Assistant provides essential operational and administrative support across all phases of clinical studies. This role ensures high...
Coopers Group AGBaselstellen-basel.ch
Clinical Trial Manager
m/f/d, Basel-Stadt
The Clinical Trial Manager serves as their region's lead and expert on complex clinical development trials to secure expeditious country level set-up, start, enrolment and quality control
Contract...
GlaxoSmithKlineSchweizappcast.io
to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate...
BeOne Medicines I GmbHBasel
importantly, share our passionate interest in fighting cancer.
General Description:
Under close supervision, CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local...
F. Hoffmann-La Roche GruppeBaselappcast.io
manager status
• Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research and biomarker groups and other members of project teams
• Lead and/or support internal...
BeOne Medicines I GmbHBasel
on a regional level
Collaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required
Represents the regional study team at internal meetings...
F. Hoffmann-La Roche AGBaselappcast.io
of Phase II and III clinical studies, collaborating with cross-functional teams on study analytics, data management, and safety profiles.* **Scientific Leadership:** Maintain the highest levels of scientific and clinical knowledge within the MS...
Lausannemichaelpage.ch
Support Clinical Project Managers in tracking study milestones and deliverables
• Maintain and oversee Trial Master File (TMF/eTMF) completeness and quality
• Prepare, review, finalize, and distribute clinical study documentation
• Participate...
Baselicims.com
Overview:
In this exciting role the successful candidate will contribute to CMC tasks from discovery/preclinical stage to clinical and potentially commercial stage. This includes managing outsourcing activities for development and manufacturing...
DebiopharmLausanneworkable.com
Collaboration: Act as a key member of the clinical study team, working closely with Clinical Trial Managers and other stakeholders in a matrix environment.
Requirements
Your profile
• Education: Scientific or technical background, ideally at a university...
RocheBaselroche.com
reports.
• Influence product safety strategy and provide vital safety input into the overarching Clinical Development strategy.
• Contribute significantly to risk management by preparing and maintaining CCDS, labeling documents (including the IB), risk...
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