Clinical Trial Manager Jobs in Zurich
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Search Results - Clinical Trial Manager Jobs in Zurich
LimmaTech Biologics AG-Zurich
LimmaTech Biologics AG in Switzerland is seeking a Clinical Project Manager (100%) to lead and manage clinical trials and programs, including Phase I/II studies. The role focuses on scope, quality, timeline and budget adherence, with emphasis...
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headcount AG-Zurich
headcount AG in Switzerland seeks a Group Lead Clinical Operations to guide a growing team of Clinical Project Managers and shape the clinical development strategy. You will oversee global Phase I/II trials, ensure on-time delivery within budget...
LimmaTech Biologics AG-Zurich
team your responsibilities will include:
• Managing clinical trials to ensure adherence to scope, quality, budget and timelines
• Preparation of high quality clinical study documentation (including but not limited to protocol, study plans, reports...
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headcount AG-Zurich
biotechnology or pharmaceuticals
• Extensive experience managing global Phase I and/or II clinical trials
• Previous experience leading Clinical Project Managers or cross‑functional clinical teams
• Strong understanding of clinical development strategy
• Proven...
Teleflex-Zurich
reports to the Clinical and Medical Affairs Peripheral Vascular Intervention head, and is responsible for managing Clinical Trials related to the peripheral portfolio. This includes the design, regulatory submission, and conduction of global clinical...
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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...
CSL Plasma Inc.-Zurich
CSL Plasma Inc. is seeking a senior scientific leader to provide input to clinical development strategies and trial design in Glattbrugg, Switzerland.
The role drives the scientific strategy across programs, authors key study documents, and mentors...
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CSL-Zurich
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable...
CSL Plasma Inc.-Zurich
the highest quality and full compliance of all outputs. Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial‑related documents and the scientific oversight of clinical trials.
You will facilitate...
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Universitätsspital Zürich USZ-Zurich
and laboratory teams to jointly define research questions, develop analytical strategies, and execute research projects
Additionally, you will contribute to prospective clinical studies and treatment trials in patients with sarcoidosis and apply advanced data...
Ultragenyx-Zurich
Rheumatology or Neurology (required).
• Academic/Faculty experience (5+ years) with a track record of high‑quality publications.
• Pharmaceutical experience in drug development and clinical trials or Medical Affairs (3+ years).
• Experience in the management...
two.jobs-Bern, 95 km from Zurich
to improving cancer treatment for the Swiss population as a non‐profit organization. Guided by our vision "Clinical research for a cure tomorrow," we conduct oncology clinical trials and serve as a key partner for authorities, professional associations...
SkyCell AG-Zurich
You'll work across two types of accounts: specialized Clinical Trial forwarders, where you'll take direct commercial ownership and global forwarders specialised in Cold Chain, where you'll build joint business plans and drive adoption from the top down...
Kinderspital Zürich-Zurich
Clinical Trials Unit Oncology
Arbeitgeber Kinderspital Zürich
Das Kinderspital Zürich ist mit rund 3'000 Mitarbeitenden das grösste Universitäts-Kinderspital der Schweiz und eines der führenden Zentren für Kinder- und Jugendmedizin in Europa. Das...
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Teleflex-Zurich
and ethics committees, with collaboration across Clinical Safety, data operations, and project management.
You will ensure compliance with ISO 14155/ MDR, work with eCRF systems and electronic trial master files, and contribute to safety reporting and
#J...
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