Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
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...
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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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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...
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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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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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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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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...
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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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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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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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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...
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Debiopharm-Lausanne
Lausanne, Switzerland
Your Mission:
As the Senior Manager of Statistical Programming, you will provide strategic leadership for Statistical and Clinical Data Science Programming. You will be the driving force behind our digitalization strategy...
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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...
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Coopers Group AG-Basel
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...
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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...
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