Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
BeiGene, Ltd.Basel
solid knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager. Supports the alignment of regional deliverables with overall study goals under the direction of the Regional Clinical Study Manager...
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...
BeiGene, Ltd.Basel
BeOne seeks a Regional Clinical Study Support Specialist to assist the Regional Clinical Study Manager in delivering regional clinical studies on time and within quality standards. You will gain hands-on experience in trial operations, from...
BeiGene, Ltd.Baselappcast.io
in fighting cancer.
Position
Regional Clinical Compliance (RCC) Inspection Manager is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials.
The role provides...
AXEPTA SAGeneva
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...
BeiGene, Ltd.Baselappcast.io
BeOne is seeking a Regional Clinical Compliance (RCC) Inspection Manager to lead proactive inspection readiness and audit support across regional and global levels. You will guide clinical teams on inspection expectations, coordinate responses...
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...
BeOne MedicinesBasel
clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effective inspection readiness programs, and successful management of inspections and audits.
Key responsibilities include...
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...
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...
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...
Universitätsspital Zürich USZZurich
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...
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...
BeOne MedicinesBasel
BeOne Medicines is seeking an RCC Inspection Lead to drive proactive risk management and sustained inspection readiness across clinical trials in the EMEA region. You will guide clinical teams, coordinate audits, and ensure timely, compliant...
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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