Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
C115 (FCRS = CH115) Sandoz Pharmaceuticals AG-Rotkreuz
Sandoz Pharmaceuticals AG in Switzerland seeks a Medical Manager to design, implement and execute Medical Affairs plans for the assigned therapy area, aligning with product strategy.
You will provide scientific information, contribute to clinical...
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headcount AG-Zurich
headcount AG in Switzerland seeks a Group Lead Clinical Operations to guide a growing team of Clinical Project Managers and shape the clinical development strategy. You will oversee global Phase I/II trials, ensure on-time delivery within budget...
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Roche Holding AG-Basel
in the pharmaceutical/healthcare industry and drug development (therapeutic area a plus), alongside a solid understanding of the clinical trial environment, ICH‑GCP, and lifecycle sequence/interdependencies.
• You are highly experienced in clinical trial management...
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headcount AG-Zurich
biotechnology or pharmaceuticals
• Extensive experience managing global Phase I and/or II clinical trials
• Previous experience leading Clinical Project Managers or cross‑functional clinical teams
• Strong understanding of clinical development strategy
• Proven...
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Debiopharm-Lausanne
Mission
The Clinical Development Quality Manager (CDQM) is responsible for ensuring quality oversight across clinical development activities and supporting the maintenance of GCP compliance. This role supports stakeholders in vendor qualification...
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Neurocrine Biosciences-Allschwil
to multidisciplinary project teams for assigned TA/Program, advises Senior Technical Leadership and Executive Management and regularly interfaces with internal and external colleagues to ensure timely and accurate dissemination of Clinical Pharmacology findings.
Your...
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Novartis Farmacéutica-Basel
Lead Biomedical Research Early Program Teams (BPTs) to enable the start of clinical development and continuing through clinical trials needed to support TDP. May lead multiple global project teams
• Integrates preclinical information (pharmacology...
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Debiopharm-Lausanne
Management functions
• Proven expertise in clinical and pharmaceutical industry experience in planning and conducting clinical trials, preferably in early phase clinical development oncology studies within a pharmaceutical industry setting
• Demonstrated...
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BD-Vilters-Wangs
to facilitate the conduct of the study.
Trial Master File (TMF) maintenance and perform study and/or site-level audits to ensure that study files are current, accurate, complete and audit-ready.
Study and site-level management of the Clinical Trial Management...
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Alentis Therapeutics-Allschwil
management:
• Develop demand forecasts and supply plans based on study protocols, clinical scenarios and enrollment projections.
• Plan, implement and execute the supply strategy for trial medication and ancillary supplies in collaboration with clinical...
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GSK-Baar
clinical studies, including real-time clinical decision-making on patient eligibility, protocol-related medical queries, and safety oversight
Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical...
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Swiss Cancer Institute-Bern
Guided by our vision "Clinical research for a cure tomorrow," we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the pharmaceutical industry. Approximately 70 employees at our Competence Center...
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Incyte-Morges
clinical trials.
Identifies, evaluates, and proactively manages clinical and program risks, implementing mitigation strategies to support program success.
Represents the organization at scientific and medical forums, including congresses, advisory boards...
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CSL Plasma Inc.-Zurich
CSL Plasma Inc. is seeking a senior scientific leader to provide input to clinical development strategies and trial design in Glattbrugg, Switzerland.
The role drives the scientific strategy across programs, authors key study documents, and mentors...
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CSL Plasma Inc.-Zurich
the highest quality and full compliance of all outputs. Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial‑related documents and the scientific oversight of clinical trials.
You will facilitate...
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