Clinical Trial Manager Jobs
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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...
headcountBasel
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...
GlaxoSmithKlineSchweizappcast.io
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...
CRISPR TherapeuticsBern
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...
Nestlé SALausanneappcast.io
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...
GlaxoSmithKlineBern
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...
1 similar job: Zug
Novartis AGRiehenjobup.ch
designed for career starters, career changers, and career relaunchers. If you are ready for two transformative years to gain hands-on experience in a diverse, multicultural, global and inclusive environment in early drug development and clinical trials...
1 similar job: Basel
gloor&lang AGZurichjoin.com
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...
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...
CSLOpfikon
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...
Hilo By AktiiaNeuchâtelworkable.com
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...
TSP, a Syneos Health companyBern
education and experience.
Graduate degree (MBA/PhD/MD) is a plus.
Proven experience in strategic sales, global business development, or client relationship management.
Significant experience in the clinical trial industry with deep knowledge...
Randstad (Schweiz) AGLausannejobup.ch
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...
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...
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...
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