Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
Roche Holding AGBaselappcast.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...
AXEPTA SAGeneva
in charge of writing clinical documents.- Verify the consistency of the different sources of evidence: IFU, risk management files, PMS data, trials and tests, labeling, vigilance, and scientific literature.- Ensure the alignment of clinical data within...
DebiopharmLausanneappcast.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...
SJP Biotec GmbHZurich
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...
CSL Plasma Inc.Zurichappcast.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...
BeiGeneBasel
across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effectiveinspectionreadiness programs, and successful management of inspections and audits.
Key responsibilities...
SJP Biotec GmbHZurich
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...
BeiGeneBasel
BeOne in Switzerland seeks an Inspection Lead to drive proactive risk management, readiness, and regulatory compliance across clinical trials. You will lead inspection readiness programs and coordinate audit responses at regional/global levels...
Neurocrine BiosciencesAllschwil
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...
AXEPTA SAGeneva
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 in drafting...
BeiGene, Ltd.Basel
BeOne is expanding and seeks an experienced RCC Inspection Lead to drive proactive risk management, rigorous readiness for regulatory inspections, and effective audits across clinical trials. You will lead regional and global inspection activities...
DebiopharmLausanne
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...
RocheBasel
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...
Rivia SAZurich
About Rivia Rivia is a data engine for clinical trial intelligence. It provides data infrastructure and AI-driven workflows for clinical trial teams, enabling biotechs to run studies more efficiently and to demonstrate which patients derive...
Neurocrine BiosciencesAllschwilappcast.io
needs.
The role requires extensive experience in drug development, regulatory strategy, and trial design, with a track record guiding projects through global regulatory submissions and risk management.
#J-18808-Ljbffr...
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