Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
CTC Resourcing Solutions-Basel-
CTC Resourcing Solutions in Switzerland is seeking a Clinical Operations Manager to lead clinical trials and Expanded Access Programs. The role demands at least 5 years of experience in clinical trial management, preferably from CRA level to global...
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Abbott Laboratories-Basel-appcast.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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CTC Resourcing Solutions-Basel-
and kept up to date
Ensures inspection readiness
Qualifications and Experience:
Relevant working/residency permit or Swiss/EU‑Citizenship required.
At least 5 years’ experience in managing clinical trials phase 1 – 3, preferably from CRA level up...
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Abbott Laboratories-Basel-appcast.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...
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Coopers Group GmbH-Basel-
Coopers Group GmbH in Basel is seeking an experienced Senior Change Management Leader/Clinical Trial to lead large-scale transformation initiatives within clinical trial oversight. This role involves acting as a strategic partner, guiding complex...
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BeiGene-Basel-
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...
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Michael Page International (Switzerland) SA-Basel-
submissions related to clinical and non‑clinical development activities, including but not limited to:
Clinical Trial Applications (CTAs)
Submissions, amendments and responses to requests for information
Orphan Drug Designation applications
Paediatric...
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Basel-icims.com-
Overall accountability for drug supply chain in preclinical and clinical trials.
Qualifications:
• PhD or MSc in Organic or Analytical Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences or related scientific discipline.
• Two (for PhD) or five...
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Novartis-Basel-
Summary
Location: Basel, Switzerland
Full time, Hybrid
At Novartis, we are re‑imagining how clinical trials are designed, delivered, and scaled—placing digital, operational data and AI at the heart of execution. As Head of GCO Technology & AI, you...
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Roche-Basel-roche.com-
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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Ctcon-Basel-stellen-basel.ch-
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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Roche-Basel-roche.com-
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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Ctcon-Basel-stellen-basel.ch-
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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Roche-Basel-roche.com-
clinical trial results so that these can potentially create value for HCPs and benefit patients.
Who You Are
You hold an advanced life-science degree (e.g., MD, PhD or PharmD). A specialization degree or industry experience in CV/metabolism is a must...
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Basel-stellen-basel.ch-
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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