Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
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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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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appcast.io -
TSP, a Syneos Health company-Basel
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...
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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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appcast.io -
Taylor Strategy Partners-Basel
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...
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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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stellen-basel.ch -
Jobup-Basel
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 for global and national label changes, including safety‑related...
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Novartis AG-Basel
in‑Human (FIH) and Phase IIa studies, working collaboratively with clinical, regulatory, biomarker, and profiling partners.
• Leads the creation of clinical components of key documents e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures...
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jobup.ch -
Abbott-Basel
and Labeling Sub‑Teams.
Ensure robust oversight of clinical activities, safety monitoring, risk management plans, and regulatory documentation.
What You’ll Bring
We recognize that career paths are not one‑size‑fits‑all, and we welcome diverse experiences...
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Roche-Basel
Catalysis (PTDC-C) department is dedicated to designing and developing robust, cost-effective drug substance processes using state-of-the-art science and methodologies. Our work supports the synthetic molecules portfolio from initial human trials through...
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roche.com -
Ctcon-Basel
and Dermatology with one of the strongest pipelines of Phase II/III studies in the world.
For our clients Global Clinical Supply (GCS) who manages the packaging, labeling and worldwide distribution of clinical finished goods, we are looking for a QA Manager...
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stellen-basel.ch -
Roche-Basel
Protocols, IBs, CSRs) and optimal resource allocation.
• Drive innovative trial design and data interpretation in close partnership with Medical and Biomarker leadership to optimize clinical development plans and dose selection.
• Influence global strategy...
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roche.com -
Ctcon-Basel
monitors and tracks data cleaning, data review, query management, and database lock; Represents Data Management (Biometry) at Clinical Trial Team (CTT) meetings, investigators and monitors meetings.
~Provides Data Management input to the development...
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stellen-basel.ch -
Roche-Basel
to millions of patients worldwide. PT is involved in producing every Roche medicine from the development process through clinical trials and continuing to product maturity. Our organization coordinates all aspects of the production of Roche medicines in all...
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roche.com -
Basel
Governance, Safety & Compliance
• Serve as an active member of Therapeutic Area Review Committees , Product Safety Teams, and Labeling Sub Teams .
• Ensure robust oversight of clinical activities, safety monitoring, risk management plans, and regulatory...
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stellen-basel.ch -
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