Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
C115 (FCRS = CH115) Sandoz Pharmaceuticals AG-Rotkreuz-appcast.io-
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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AXEPTA SA-Geneva-
of evidence: IFU, risk management files, PMS data, trials and tests, labelling, complaints, vigilance and scientific literature.
• Ensure the alignment of clinical data within all regulatory documentation.
• Train and support the external providers involved...
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Roche Holding AG-Basel-appcast.io-
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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SJP Biotec GmbH-Zurich-
development field - RAS/eIF4A/translation-pathway inhibition.
Key Responsibilities
Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
Lead and manage all clinical development activities...
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Debiopharm-Lausanne-appcast.io-
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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Alentis Therapeutics-Allschwil-join.com-
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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SJP Biotec GmbH-Zurich-
Key Responsibilities
• Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
• Lead and manage all clinical development activities across the SJP portfolio
• Design Phase 2 and 3...
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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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MEDICJOBS-Zurich-
and laboratory teams to jointly define research questions, develop analytical strategies, and execute research projects
• Additionally, you will contribute to prospective clinical studies and treatment trials in patients with sarcoidosis and apply advanced data...
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Incyte-Morges-
Incyte is seeking a senior clinical development leader to implement early development programs for dermatology, immunology, and rheumatology assets. This role involves shaping translational strategies, coordinating cross-functional teams, managing...
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Universitätsspital Zürich USZ-Zurich-
and laboratory teams to jointly define research questions, develop analytical strategies, and execute research projects
• Additionally, you will contribute to prospective clinical studies and treatment trials in patients with sarcoidosis and apply advanced data...
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Incyte-Morges-
agents.
Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound.
Acts as subject matter expert for business development activities...
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CSL Plasma Inc.-Zurich-appcast.io-
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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Elan Personal AG-Basel-
clinical decision-making. To meet the diverse measurement needs across clinical trials, the organization collaborates with multiple third-party DHT manufacturers. While DHTs provide critical evidence, their implementation requires specialized technical...
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CSL Plasma Inc.-Zurich-appcast.io-
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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