Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
Flexsis-Allschwil
and management of study committees
Scientific input to IRB/EC and Health Authority responses
Participation in scientific discussions with external experts
Training of internal stakeholders on scientific aspects of the trial
Contribution to broader clinical...
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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...
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CTC Resourcing Solutions-Basel
Location & Contract
Allschwil, Switzerland. Contract duration: 2 years.
Responsibilities
Act as a core member of the Clinical Trial Team (CTT) and collaborate closely with the Clinical Trial Physician.
Scientific planning, conduct, data review...
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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...
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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...
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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...
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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...
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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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Flexsis-Allschwil
stakeholders
Generates trial metrics and status reports
Represents Data Management at Clinical Trial Team (CTT) meetings
Presents trial related topics at CTT, Investigators and Monitors meetings
Manages and is accountable for Data Management activities...
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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...
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stellen-basel.ch -
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...
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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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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...
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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...
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