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Clinical Trial Manager Jobs

1 - 15 of 55
1 - 15 of 55
Search Results - Clinical Trial Manager Jobs
InGoedeBanen.nl-Lausanne
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...
headcount-Basel
headcount is seeking a Clinical Scientist in Basel, Switzerland for a 12-month contract. This position focuses on clinical trial data cleaning and data review for ongoing Phase II studies. Candidates should have 3–5 years in clinical data management...
InGoedeBanen.nl-Lausanne
role within the Nestlé Health Science Supply Operations team. This position is responsible for defined aspects of Investigational Medicinal Products (IMP), Investigational Nutritional Products (INP), Clinical Trial Materials (CTM), and ancillary...
CRISPR Therapeutics-Bern
will ensure accurate, consistent, high quality, and complete data.The successful candidate will provide clinical data management oversight of outsourced clinical trials, including but not limited to: project management, vendor management, coordination...
GlaxoSmithKline-Schweiz
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...
appcast.io -
gloor&lang AG-Zurich
This role is suited for early to mid-career professionals with experience in clinical trials and GCP-based quality environments. It is a hands-on specialist role without management responsibility. Responsibilities  •  Support clinical quality oversight...
join.com -
GlaxoSmithKline-Bern
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 ability to incorporate...
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Hilo By Aktiia-Neuchâtel
for Electronics and Microtechnology (CSEM) - is the world’s only medically accurate, continuous blood pressure monitor that is cuffless in daily life in the consumer space. Validated through extensive clinical trials and CE Marked as a Class IIa medical device...
workable.com -
CSL-Opfikon
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The Associate Director provides for statistical excellence in clinical development plans, trial...
Aenova Group / SwissCo Services AG-Sisseln
f/m/d) Your key responsibilities Supervision, organization, and coordination of the manufacture of preclinical trials as well as clinical investigational medicinal products (IMPs) in development projects in accordance with the applicable GMP guidelines...
Ridgeline Discovery-Basel
and communication of clinical trial data from clinical trials Author and develop clinical documents like, clinical study protocols and amendments and review other clinical documents like safety management plan, medical monitoring plan Work closely with colleagues...
Aenova Group / SwissCo Services AG-Sisseln
Your key responsibilities  •  Supervision, organization, and coordination of the manufacture of preclinical trials as well as clinical investigational medicinal products (IMPs) in development projects in accordance with the applicable GMP guidelines...
Abbott Laboratories-Basel
to PSURs, clinical overviews, and risk management plans  •  As part of the Labeling Sub‑Team, provide medical input and scientific strategies for global and national label changes, including safety‑related updates  •  Ensure that all medical and promotional...
appcast.io -
CSL Behring-Bern
The Senior Laboratory Specialist, Tech Ops researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monitors and ensures products meet...
Abbott Laboratories-Basel
Act as a core member of the Product Safety Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk‑management plans  •  As part of the Labeling Sub‑Team, provide medical input and scientific strategies...
appcast.io -
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