Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
Skilled Recruitment Solutions GmbHLiestal
Skilled Recruitment Solutions GmbH is seeking a Global Clinical Trial Manager to oversee the planning, execution, and closeout of clinical trials in Basel-Landschaft, Switzerland. Responsibilities include managing project budgets, leading trial...
InGoedeBanen.nlLausanne
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...
Skilled Recruitment Solutions GmbHLiestal
the (e)TMF is correctly established, regularly reviewed for completeness, and kept up to date
Ihr Profil
Professional Experience: Minimum of 5 years in managing clinical trials (Phases I–III), ideally with a career progression from CRA to Global...
InGoedeBanen.nlLausanne
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...
Neurocrine BiosciencesAllschwil
development, with strong leadership and analytical skills. Responsibilities include directing clinical trials, implementing study protocols, and maintaining communication with senior management. The position is based in Allschwil, Switzerland and offers...
Nestlé SALausanneappcast.io
nutrition, or CRO settings)
• 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...
Aenova Group / SwissCo Services AGSisseln
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...
Neurocrine BiosciencesAllschwil
and late stages of clinical development
Oversees the clinical trials program in conjunction with the Clinical Operations
Analyzes, interprets, and presents results of clinical studies to internal and external audiences as directed by Senior Management...
Aenova Group / SwissCo Services AGSisseln
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...
Taylor Strategy PartnersBasel
extensive experience in clinical research and commercialization
Graduade degree (MBA/PhD/MD degrees) is a plus
Significant experience in the clinical trial industry, with deep knowledge of the pharmaceutical landscape—required.
Demonstrated success...
Abbott LaboratoriesBaselappcast.io
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...
BeiGeneBasel
Trial Management Systems
Other Qualifications:
• Proven Project Management experience in Global Clinical Studies (Oncology experience preferred)
• Advanced knowledge of clinical operations methodologies, in depth understanding of all aspects...
Abbott LaboratoriesBaselappcast.io
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...
Coopers Group AGBaselstellen-basel.ch
Change Management Lead/Clinical Trials NOVPJP00004484
m/f/d, Basel-Stadt
We are looking for an experienced Senior Change Management Leader/Clinical Trial to drive large-scale transformation initiatives across clinical trial oversight . This role...
DebiopharmLausanneworkable.com
Experience: At least 3 years in the pharmaceutical industry, with hands-on experience in clinical trials and TMF documentation/systems.
• Expertise: Solid knowledge of Good Clinical Practice (GCP) and advanced proficiency in managing digital clinical...
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