Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
CTC Resourcing Solutions-Basel-
Equivalent relevant experience in Regulatory Affairs operations or eTMF management may be considered in place of formal education
Min. 2 years’ experience in Regulatory Affairs, Regulatory Operations, or Clinical Trial Documentation
Min. 2 years’ experience...
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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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Monte Rosa Therapeutics-Basel-
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 (for MSc) years of experience...
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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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Novartis AG-Basel-jobup.ch-
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-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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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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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-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-
development plans from Phase 1 through Phase 2 (proof-of-concept)
Coach Clinical Scientists in a line- or functional-manager status
Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics...
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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-
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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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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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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