Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
LimmaTech Biologics AG-Zurich-appcast.io-
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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RM IT Professional Resources AG-Basel-
in early clinical development. Operational project management experience including excellent planning, prioritization, problem solving and organizational skills.
• Track record of successfully managing multiple clinical trials concurrently. Used to managing...
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206030 Fresenius Kabi SwissBioSim GmbH-Eysins-appcast.io-
cross-functional teams jointly achieve trial objectives and goals.
• Understand agency requirements related to clinical packages and plans, managing functions such as CSR, TFLs, ISS, etc.
• Ensure inspection readiness and manage CAPAs related to clinical...
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RM IT Professional Resources AG-Basel-
environment.
• Strong understanding of clinical trial methodology, ICH-GCP and relevant regulatory requirements.
• Proven experience in operational project management, including planning, prioritisation and problem solving.
• Ability to interpret trial-level...
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Witzig The Office Company AG-Allschwil-appcast.io-
The Clinical Supply Manager is accountable for management, coordination and efficient on-time delivery of trial supplies (including IMP= Investigational Medicinal Product, Placebo, Standard of Care and clinical ancillaries) for global clinical...
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Merck Healthcare-Eysins-
responsible for driving excellence in the planning, execution, and oversight of clinical trial monitoring and site management activities. The role is pivotal in ensuring that clinical monitoring and site management practices are globally harmonized, inspection...
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Colgate-Palmolive Company-Therwil-
and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.
Clinical Research Manager
Job Details...
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ELAN Personal AG-Basel-
project and budget management, SAP proficiency, and leadership across cross-functional teams to ensure timely, high-quality clinical supply delivery for global trials.
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LimmaTech Biologics AG-Zurich-appcast.io-
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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ELAN Personal AG-Basel-
Site Manager 80-100%
Background:
This role is responsible for the operational and strategic management of clinical drug labeling, packaging, and device assembly outsourced to a global network of Contract Manufacturing Organizations (CMOs). Operating...
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206030 Fresenius Kabi SwissBioSim GmbH-Eysins-appcast.io-
global trials, manage cross‑functional teams and CROs, and ensure timelines, budgets, and quality meet corporate expectations.
Fluency in English, an advanced life sciences degree, and at least 7 years in industry clinical research are required.
#J...
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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...
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HUG - Hôpitaux Universitaires de Genève-Chêne-Bourg-
in clinical research, such as a Diploma X Studies-DAS, continuing education in Management of Clinical Trials, that Inter-University (DIU) of to clinical trials of drugs (FIEC) or a deemed equivalent.
You justify at least five years of experience in the field...
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Merck-Eysins-
Merck is seeking a Clinical Site Management Excellence Lead to drive strategic and operational leadership in monitoring and site management for global trials. The role emphasizes harmonized, inspection-ready processes and collaboration across CROs...
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AXEPTA SA-Geneva-
of evidence : IFU, risk management files, PMS data, trials and tests, labelling, complaints, vigilance and scientific literature.
Ensure the alignment of
clinical data
within all regulatory documentation.
Train and support the
external providers
involved...
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