Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
CTC Resourcing Solutions-Basel
of whom have given us some great feedback from their time working there.
Purpose
Participates in the planning and execution of one or more clinical trials or Expanded Access Programs including preparation of trial documents, management of Trial Master...
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...
CTC Resourcing Solutions-Allschwil
in the search for a
Clinical Trial Scientist.
The role is in
Allschwil, Switzerland . The contract duration is
2 years .
Your Main Responsibilities
Act as a core member of the Clinical Trial Team (CTT) and collaborate closely with the Clinical Trial...
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...
CTC Resourcing Solutions-Basel
CTC Resourcing Solutions is seeking an experienced Clinical Trials Manager for a 6-month maternity cover in Basel, Switzerland. The role involves planning, execution, and oversight of clinical trials, ensuring compliance with ICH-GCP standards...
HUG - Hôpitaux Universitaires de Genève-Geneva
Assistant at the Department of Clinical Pharmacology and Toxicology – 80% to 100%The clinical research assistant plays a key role in the management, the and the implementation of research studies conducted within the Department of Clinical Pharmacology...
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...
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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...
F. Hoffmann-La Roche Gruppe-Basel
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...
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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...
Nestlé SA-Lausanne
Experience and proven impact in leading safety management in complex clinical trials, including issue management and regulatory frameworks of nutrition and medical nutrition
• Expertise in preparation of clinical safety assessments and regulatory submissions...
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Merck Healthcare-Eysins
knowledge and experience in clinical trial management including managerial responsibility.
Expert experience in multiple Therapeutic Areas.
Requires extensive professional experience in relevant disciplines and substantial project management experience...
Coopers Group AG-Basel
for the collection and delivery of clinical trial samples (e.g. Safety, Chemistry, Biomarker, PK and PD) across the portfolio of trials. The BOL is an integral part of the Clinical Trial Team and provides operational/ project management expertise as it relates...
stellen-basel.ch -
Novartis-Basel
drug development process, Translational Medicine departments, clinical trial process, and the tools and technical platforms you’ll use.
Throughout the program, fellows reunite for continuous learning focused on soft skills, cross‑functional exposure...
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...
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